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Phosphoramidites

2'-Modified Phosphoramidites
(535/535)
2'-Phosphoramidites
(27/27)
3'-Modified Phosphoramidites
(201/201)
5'-Modified Phosphoramidites
(34/34)
Arabino Phosphoramidites
(24/24)
Base Protected Phosphoramidites (423/423) Dye Phosphoramidites
(64/64)
Label Phosphoramidites
(81/81)
Linker Phosphoramidites
(91/91)
Other Phosphoramidites
(93/93)
PMO Phosphoramidates and Derivatives (33/33) PseudoUridine Phosphoramidite
(12/12)
Reverse Phosphoramidites
(25/25)
Spacer Phosphoramidites
(24/24)
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N4-Ethyl Cytidine CED phosphoramidite

Description: N4-Ethyl Cytidine CED phosphoramidite is a chemical compound used in the synthesis of nucleic acids, particularly RNA molecules. It consists of a cytidine nucleoside modified with a tert-butyldimethylsilyl (TBDMS) group at the 2' position and an ethyl group at the N4 position. Additionally, it contains a CED (2-cyanoethyl diisopropylphosphoramidite) moiety, which serves as a protecting group during the synthesis process. This phosphoramidite derivative allows for efficient and selective incorporation of the modified cytidine into the growing RNA chain during solid-phase synthesis, enabling researchers to tailor RNA molecules with specific functionalities for various biological and therapeutic applications.
CAT: BRP-01303
Molecular Formula: C47H66N5O8PSi
Molecular Weight: 888.12
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InChIKey: YLWRTGHURVFSCS-UODQAQMXSA-N
IUPAC Name: (2R,3R,4R,5R)-2-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-4-((tert-butyldimethylsilyl)oxy)-5-(4-(ethylamino)-2-oxopyrimidin-1(2H)-yl)tetrahydrofuran-3-yl (2-cyanoethyl) diisopropylphosphoramidite
InChI: InChI=1S/C47H66N5O8PSi/c1-13-49-41-28-30-51(45(53)50-41)44-43(60-62(11,12)46(6,7)8)42(59-61(57-31-17-29-48)52(33(2)3)34(4)5)40(58-44)32-56-47(35-18-15-14-16-19-35,36-20-24-38(54-9)25-21-36)37-22-26-39(55-10)27-23-37/h14-16,18-28,30,33-34,40,42-44H,13,17,31-32H2,1-12H3,(H,49,50,53)/t40-,42-,43-,44-,61?/m1/s1
Synonyms: 2'-TBDMS Cytidine(ethyl) 3'-CE-phosphoramidite; N4-Ethyl Cytidine 3'-tBDSilyl CED phosphoramidite; N4-Ethyl Cytidine 2'-tBDSilyl CED phosphoramidite

4-Thio Uridine CED phosphoramidite

Description: 4-Thio Uridine CED phosphoramidite is a compound used in the chemical synthesis of nucleic acids, particularly RNA molecules. It consists of a uridine nucleoside modified with a 2'-TBDMS (tert-butyldimethylsilyl) group at the 2' position and a 4-S-(2-cyanoethyl) modification. Additionally, it contains a CE (2-cyanoethyl) phosphoramidite moiety, which serves as a protecting group during the synthesis process. This phosphoramidite derivative allows for efficient and selective incorporation of the modified uridine into the growing RNA chain during solid-phase synthesis, enabling researchers to tailor RNA molecules with specific functionalities for various biological and therapeutic applications.
CAT: BRP-01305
CAS: 154665-04-0
Molecular Formula: C48H64N5O8PSSi
Molecular Weight: 930.18
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InChIKey: DKQKZAVAXOCNNU-CRHOWCKESA-N
CanonicalSMILES: CC(C)N(C(C)C)P(OCCC#N)OC1C(OC(C1O[Si](C)(C)C(C)(C)C)N2C=CC(=NC2=O)SCCC#N)COC(C3=CC=CC=C3)(C4=CC=C(C=C4)OC)C5=CC=C(C=C5)OC
IUPAC Name: 3-[[(2R,3R,4R,5R)-2-[[bis(4-methoxyphenyl)-phenylmethoxy]methyl]-4-[tert-butyl(dimethyl)silyl]oxy-5-[4-(2-cyanoethylsulfanyl)-2-oxopyrimidin-1-yl]oxolan-3-yl]oxy-[di(propan-2-yl)amino]phosphanyl]oxypropanenitrile
InChI: InChI=1S/C48H64N5O8PSSi/c1-34(2)53(35(3)4)62(58-31-15-28-49)60-43-41(59-45(44(43)61-64(10,11)47(5,6)7)52-30-27-42(51-46(52)54)63-32-16-29-50)33-57-48(36-17-13-12-14-18-36,37-19-23-39(55-8)24-20-37)38-21-25-40(56-9)26-22-38/h12-14,17-27,30,34-35,41,43-45H,15-16,31-33H2,1-11H3/t41-,43-,44-,45-,62?/m1/s1
Synonyms: Uridine, 5'-O-[bis(4-methoxyphenyl)phenylmethyl]-4-S-(2-cyanoethyl)-2'-O-[(1,1-dimethylethyl)dimethylsilyl]-4-thio-, 3'-[2-cyanoethyl N,N-bis(1-methylethyl)phosphoramidite]; Uridine, 5'-O-[bis(4-methoxyphenyl)phenylmethyl]-4-S-(2-cyanoethyl)-2'-O-[(1,1-dimethylethyl)dimethylsilyl]-4-thio-, 3'-[2-cyanoethyl bis(1-methylethyl)phosphoramidite]; 4-S-(2-cyanoethyl)-2'-TBDMS-U 3'-CE-phosphoramidite

MMT-2'-tBDSilyl Adenosine (n-bz) CED phosphoramidite

Description: MMT-2'-tBDSilyl Adenosine (n-bz) CED phosphoramidite is a specialized reagent utilized in oligonucleotide synthesis. It comprises an adenosine nucleoside modified with a 2'-tBDSilyl group and protected with a benzoyl (n-bz) group. Additionally, it contains a CED (2-cyanoethyl diisopropylphosphoramidite) moiety, which serves as a protecting group during the synthesis process. The MMT (Monomethoxytrityl) group is typically used for temporary protection of hydroxyl groups in nucleosides. This phosphoramidite derivative enables efficient and selective incorporation of the modified adenosine into the growing nucleotide chain during solid-phase synthesis. It plays a crucial role in the design and synthesis of modified oligonucleotides for various applications in molecular biology, diagnostics, and therapeutics.
CAT: BRP-01320
CAS: 135711-69-2
Molecular Formula: C52H64N7O7PSi
Molecular Weight: 958.17
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InChIKey: VMFYLWGANHVWAU-LTMMGAFGSA-N
CanonicalSMILES: CC(C)N(C(C)C)P(OCCC#N)OC1C(OC(C1O[Si](C)(C)C(C)(C)C)N2C=NC3=C(N=CN=C32)NC(=O)C4=CC=CC=C4)COC(C5=CC=CC=C5)(C6=CC=CC=C6)C7=CC=C(C=C7)OC
IUPAC Name: N-[9-[(2R,3R,4R,5R)-3-[tert-butyl(dimethyl)silyl]oxy-4-[2-cyanoethoxy-[di(propan-2-yl)amino]phosphanyl]oxy-5-[[(4-methoxyphenyl)-diphenylmethoxy]methyl]oxolan-2-yl]purin-6-yl]benzamide
InChI: InChI=1S/C52H64N7O7PSi/c1-36(2)59(37(3)4)67(63-32-20-31-53)65-45-43(33-62-52(39-23-16-12-17-24-39,40-25-18-13-19-26-40)41-27-29-42(61-8)30-28-41)64-50(46(45)66-68(9,10)51(5,6)7)58-35-56-44-47(54-34-55-48(44)58)57-49(60)38-21-14-11-15-22-38/h11-19,21-30,34-37,43,45-46,50H,20,32-33H2,1-10H3,(H,54,55,57,60)/t43-,45-,46-,50-,67?/m1/s1
Synonyms: 5'-MMT-2'-TBDMS A(Bz) 3'-CE phosphoramidite; Adenosine, N-benzoyl-2'-O-[(1,1-dimethylethyl)dimethylsilyl]-5'-O-[(4-methoxyphenyl)diphenylmethyl]-, 3'-[2-cyanoethyl bis(1-methylethyl)phosphoramidite]

MMT-2'-tBDSilyl Guanosine (n-ibu) CED phosphoramidite

Description: MMT-2'-tBDSilyl Guanosine (n-ibu) CED phosphoramidite is a specialized reagent used in oligonucleotide synthesis. It consists of a guanosine nucleoside modified with a 2'-tBDSilyl group and protected with an isobutyryl (n-ibu) group. Additionally, it contains a CED (2-cyanoethyl diisopropylphosphoramidite) moiety, which acts as a protecting group during the synthesis process. The MMT (Monomethoxytrityl) group is typically employed for temporary protection of hydroxyl groups in nucleosides. This phosphoramidite derivative facilitates efficient and selective incorporation of the modified guanosine into the growing nucleotide chain during solid-phase synthesis. It is essential for designing and synthesizing modified oligonucleotides for various applications in molecular biology, diagnostics, and therapeutics.
CAT: BRP-01321
Molecular Formula: C49H66N7O8PSi
Molecular Weight: 940.15
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InChIKey: XJHPFJYSMMSOCC-VKFKYRIUSA-N
IUPAC Name: (2R,3R,4R,5R)-4-((tert-butyldimethylsilyl)oxy)-5-(2-isobutyramido-6-oxo-1,6-dihydro-9H-purin-9-yl)-2-(((4-methoxyphenyl)diphenylmethoxy)methyl)tetrahydrofuran-3-yl (2-cyanoethyl) diisopropylphosphoramidite
InChI: InChI=1S/C49H66N7O8PSi/c1-32(2)44(57)53-47-52-43-40(45(58)54-47)51-31-55(43)46-42(64-66(11,12)48(7,8)9)41(63-65(61-29-19-28-50)56(33(3)4)34(5)6)39(62-46)30-60-49(35-20-15-13-16-21-35,36-22-17-14-18-23-36)37-24-26-38(59-10)27-25-37/h13-18,20-27,31-34,39,41-42,46H,19,29-30H2,1-12H3,(H2,52,53,54,57,58)/t39-,41-,42-,46-,65?/m1/s1
Synonyms: 5'-MMT-2'-TBDMS G(iBu) 3'-CE phosphoramidite

MMT-2'-tBDSilyl Guanosine (n-PAC) CED phosphoramidite

Description: MMT-2'-tBDSilyl Guanosine (n-PAC) CED phosphoramidite is used in oligonucleotide synthesis. It comprises a guanosine nucleoside modified with a 2'-tBDSilyl group and protected with a PAC (phenoxyacetyl) group. Additionally, it contains a CED (2-cyanoethyl diisopropylphosphoramidite) moiety, serving as a protecting group during synthesis. The MMT (Monomethoxytrityl) group temporarily shields hydroxyl groups in nucleosides. This phosphoramidite derivative facilitates efficient and selective incorporation of the modified guanosine into oligonucleotide sequences during solid-phase synthesis, crucial for tailored oligonucleotide design in various biological applications.
CAT: BRP-01322
Molecular Formula: C53H66N7O9PSi
Molecular Weight: 1004.19
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InChIKey: MBHPUJWVPHGMKR-NTWXHQQMSA-N
IUPAC Name: (2R,3R,4R,5R)-4-((tert-butyldimethylsilyl)oxy)-2-(((4-methoxyphenyl)diphenylmethoxy)methyl)-5-(6-oxo-2-(2-phenoxyacetamido)-1,6-dihydro-9H-purin-9-yl)tetrahydrofuran-3-yl (2-cyanoethyl) diisopropylphosphoramidite
InChI: InChI=1S/C53H66N7O9PSi/c1-36(2)60(37(3)4)70(66-32-20-31-54)68-46-43(33-65-53(38-21-14-11-15-22-38,39-23-16-12-17-24-39)40-27-29-41(63-8)30-28-40)67-50(47(46)69-71(9,10)52(5,6)7)59-35-55-45-48(59)57-51(58-49(45)62)56-44(61)34-64-42-25-18-13-19-26-42/h11-19,21-30,35-37,43,46-47,50H,20,32-34H2,1-10H3,(H2,56,57,58,61,62)/t43-,46-,47-,50-,70?/m1/s1
Synonyms: 5'-MMT-2'-TBDMS G(Pac) 3'-CE phosphoramidite

MMT-2'-tBDSilyl Adenosine (n-PAC) CED phosphoramidite

Description: MMT-2'-tBDSilyl Adenosine (n-PAC) CED phosphoramidite is utilized in oligonucleotide synthesis. It involves an adenosine nucleoside modified with a 2'-tBDSilyl group and protected with a PAC (phenoxyacetyl) group, coupled with a CED (2-cyanoethyl diisopropylphosphoramidite) moiety. The MMT (Monomethoxytrityl) group is typically used for temporary protection of hydroxyl groups in nucleosides. This phosphoramidite derivative enables efficient and selective incorporation of the modified adenosine into oligonucleotide sequences during solid-phase synthesis, essential for customized oligonucleotide design in various biological applications.
CAT: BRP-01323
Molecular Formula: C53H66N7O8PSi
Molecular Weight: 988.19
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InChIKey: HVOWVANSACUJFY-RPWAFYAOSA-N
IUPAC Name: (2R,3R,4R,5R)-4-((tert-butyldimethylsilyl)oxy)-2-(((4-methoxyphenyl)diphenylmethoxy)methyl)-5-(6-(2-phenoxyacetamido)-9H-purin-9-yl)tetrahydrofuran-3-yl (2-cyanoethyl) diisopropylphosphoramidite
InChI: InChI=1S/C53H66N7O8PSi/c1-37(2)60(38(3)4)69(65-32-20-31-54)67-47-44(33-64-53(39-21-14-11-15-22-39,40-23-16-12-17-24-40)41-27-29-42(62-8)30-28-41)66-51(48(47)68-70(9,10)52(5,6)7)59-36-57-46-49(55-35-56-50(46)59)58-45(61)34-63-43-25-18-13-19-26-43/h11-19,21-30,35-38,44,47-48,51H,20,32-34H2,1-10H3,(H,55,56,58,61)/t44-,47-,48-,51-,69?/m1/s1
Synonyms: 5'-MMT-2'-TBDMS A(Pac) 3'-CE phosphoramidite

N2-Isobutyryl-2'-tert-butyldimethylsilyl-7-deaza-5'-O-DMT-guanosine 3'-CE phosphoramidite

Description: N2-Isobutyryl-2'-tert-butyldimethylsilyl-7-deaza-5'-O-DMT-guanosine 3'-CE phosphoramidite is a specialized reagent used in oligonucleotide synthesis. It consists of a guanosine nucleoside modified at the N2 position with an isobutyryl group, at the 2' position with a tert-butyldimethylsilyl group, and at the 5' position with a DMT (dimethoxytrityl) group. Additionally, it contains a CE (2-cyanoethyl) phosphoramidite moiety, which serves as a protecting group during the synthesis process. This phosphoramidite derivative enables the efficient and selective incorporation of the modified guanosine into the growing nucleotide chain during solid-phase synthesis. It is crucial in the design and synthesis of modified oligonucleotides for various applications in molecular biology, genetics, diagnostics, and therapeutics.
CAT: BRP-01326
CAS: 1220889-83-7
Molecular Formula: C51H69N6O9PSi
Molecular Weight: 969.19
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InChIKey: ONYAZCDFEDIGRJ-DGMLWHETSA-N
CanonicalSMILES: N#CCCOP(OC1C(OC(N2C=CC=3C(=O)N=C(NC(=O)C(C)C)NC32)C1O[Si](C)(C)C(C)(C)C)COC(C=4C=CC=CC4)(C5=CC=C(OC)C=C5)C6=CC=C(OC)C=C6)N(C(C)C)C(C)C
IUPAC Name: (2R,3R,4R,5R)-2-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-4-((tert-butyldimethylsilyl)oxy)-5-(2-isobutyramido-4-oxo-3,4-dihydro-7H-pyrrolo[2,3-d]pyrimidin-7-yl)tetrahydrofuran-3-yl (2-cyanoethyl) diisopropylphosphoramidite
InChI: InChI=1S/C51H69N6O9PSi/c1-33(2)46(58)54-49-53-45-41(47(59)55-49)28-30-56(45)48-44(66-68(12,13)50(7,8)9)43(65-67(63-31-17-29-52)57(34(3)4)35(5)6)42(64-48)32-62-51(36-18-15-14-16-19-36,37-20-24-39(60-10)25-21-37)38-22-26-40(61-11)27-23-38/h14-16,18-28,30,33-35,42-44,48H,17,31-32H2,1-13H3,(H2,53,54,55,58,59)/t42-,43-,44-,48-,67?/m1/s1
Synonyms: N-[7-[5-O-[Bis(4-methoxyphenyl)phenylmethyl]-3-O-[[bis(1-methylethyl)amino](2-cyanoethoxy)phosphino]-2-O-[(1,1-dimethylethyl)dimethylsilyl]-β-D-ribofuranosyl]-4,7-dihydro-4-oxo-3H-pyrrolo[2,3-d]pyrimidin-2-yl]-2-methylpropanamide; 7-Deaza Guanosine CED phosphoramidite; 7-Deaza 2'-TDDMS Guanosine(iBu) 3'-CE phosphoramidite

8-Oxo-5'-DMT-2'-TBDMS Guanosine(iBu) 3'-CE Phosphoramidite

Description: 8-Oxo-2'-tBDSilyl Guanosine CED Phosphoramidite is a specialized reagent utilized in oligonucleotide synthesis. It comprises a guanosine nucleoside modified with an 8-oxo group at the 8-position of the purine ring, protected with a TBDMS (tert-butyldimethylsilyl) group at the 2'-position, and with an isobutyryl (n-iBu) group. Additionally, it contains a phosphoramidite moiety with a CE (cyanoethyl) group, serving as a protecting group during synthesis. This phosphoramidite derivative enables precise and efficient incorporation of the modified guanosine into the growing nucleotide chain during solid-phase synthesis. The presence of the 8-oxo modification is significant for investigating oxidative stress, DNA damage, and RNA modification processes.
CAT: BRP-01327
Molecular Formula: C49H67N8O9PSi
Molecular Weight: 971.16
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InChIKey: OUWOXJVBKDMSKC-NHXVREKOSA-N
IUPAC Name: (2R,3R,4R,5R)-2-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-4-((tert-butyldimethylsilyl)oxy)-5-(2-(((dimethylamino)methylene)amino)-6,8-dioxo-1,6,7,8-tetrahydro-9H-purin-9-yl)tetrahydrofuran-3-yl (2-cyanoethyl) diisopropylphosphoramidite
InChI: InChI=1S/C49H67N8O9PSi/c1-32(2)57(33(3)4)67(63-29-17-28-50)65-41-39(30-62-49(34-18-15-14-16-19-34,35-20-24-37(60-10)25-21-35)36-22-26-38(61-11)27-23-36)64-45(42(41)66-68(12,13)48(5,6)7)56-43-40(52-47(56)59)44(58)54-46(53-43)51-31-55(8)9/h14-16,18-27,31-33,39,41-42,45H,17,29-30H2,1-13H3,(H,52,59)(H,53,54,58)/t39-,41-,42-,45-,67?/m1/s1
Synonyms: 8-Oxo-2'-tBDSilyl Guanosine CED Phosphoramidite

Fmoc-Amino-DMT C-3 CED phosphoramidite

Description: Fmoc-Amino-DMT C-3 CED phosphoramidite is a specialized compound used in oligonucleotide synthesis. It features an Fmoc-protected amino group, a DMT group for 5' hydroxyl protection, and a C-3 spacer linked to a cyanoethyl diisopropyl (CED) phosphoramidite group. This compound enables the controlled addition of amino functionalities to oligonucleotides, facilitating further chemical modifications or conjugations for various research and diagnostic applications.
CAT: BRP-01334
CAS: 146918-92-5
Molecular Formula: C48H54N3O7P
Molecular Weight: 815.93
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InChIKey: JGNRMZONTWRREU-UHFFFAOYSA-N
CanonicalSMILES: N#CCCOP(OC(COC(C=1C=CC=CC1)(C2=CC=C(OC)C=C2)C3=CC=C(OC)C=C3)CNC(=O)OCC4C=5C=CC=CC5C=6C=CC=CC64)N(C(C)C)C(C)C
IUPAC Name: (9H-fluoren-9-yl)methyl (3-(bis(4-methoxyphenyl)(phenyl)methoxy)-2-(((2-cyanoethoxy)(diisopropylamino)phosphaneyl)oxy)propyl)carbamate
InChI: InChI=1S/C48H54N3O7P/c1-34(2)51(35(3)4)59(57-30-14-29-49)58-41(31-50-47(52)55-33-46-44-19-12-10-17-42(44)43-18-11-13-20-45(43)46)32-56-48(36-15-8-7-9-16-36,37-21-25-39(53-5)26-22-37)38-23-27-40(54-6)28-24-38/h7-13,15-28,34-35,41,46H,14,30-33H2,1-6H3,(H,50,52)
Synonyms: 5-Oxa-2,7-diaza-6-phosphanonanoic acid, 4-[[bis(4-methoxyphenyl)phenylmethoxy]methyl]-6-(2-cyanoethoxy)-8-methyl-7-(1-methylethyl)-, 9H-fluoren-9-ylmethyl ester; 5,7-Dioxa-2-aza-6-phosphanonanoic acid, 4-[[bis(4-methoxyphenyl)phenylmethoxy]methyl]-6-[bis(1-methylethyl)amino]-9-cyano-, 9H-fluoren-9-ylmethyl ester; 9H-Fluoren-9-ylmethyl 4-[[bis(4-methoxyphenyl)phenylmethoxy]methyl]-6-(2-cyanoethoxy)-8-methyl-7-(1-methylethyl)-5-oxa-2,7-diaza-6-phosphanonanoate

TFA-Amino C-4 CED phosphoramidite

Description: TFA-Amino C-4 CED phosphoramidite is a specialized compound used in oligonucleotide synthesis. It contains a trifluoroacetyl (TFA)-protected amino group, a C-4 spacer, and a cyanoethyl diisopropyl (CED) phosphoramidite group. This compound facilitates controlled addition of amino functionalities to oligonucleotides, enabling further chemical modifications or conjugations for various research and diagnostic applications.
CAT: BRP-01335
CAS: 936471-68-0
Molecular Formula: C15H27F3N3O3P
Molecular Weight: 385.26
Purity: ≥97%
Appearance: Colourless oily matter
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Storage: Store at -20 °C
InChIKey: XYETVXUHNJIELA-UHFFFAOYSA-N
CanonicalSMILES: N#CCCOP(OCCCCNC(=O)C(F)(F)F)N(C(C)C)C(C)C
IUPAC Name: 2-cyanoethyl (4-(2,2,2-trifluoroacetamido)butyl) diisopropylphosphoramidite
InChI: InChI=1S/C15H27F3N3O3P/c1-12(2)21(13(3)4)25(24-11-7-8-19)23-10-6-5-9-20-14(22)15(16,17)18/h12-13H,5-7,9-11H2,1-4H3,(H,20,22)
Synonyms: Phosphoramidous acid, N,N-bis(1-methylethyl)-, 2-cyanoethyl 4-[(2,2,2-trifluoroacetyl)amino]butyl ester; 2-Cyanoethyl 4-[(2,2,2-trifluoroacetyl)amino]butyl N,N-bis(1-methylethyl)phosphoramidite; 5'-Amino-Modifier C4-TFA Phosphoramidite

Fmoc-Amino C-6 3'-CE phosphoramidite

Description: Fmoc-Amino C-6 3'-CE phosphoramidite is a compound used in oligonucleotide synthesis. It features an Fmoc-protected amino group, attached to a C-6 spacer, and a 3'-cyanoethyl (3'-CE) phosphoramidite group. This compound enables the controlled addition of amino functionalities to oligonucleotides, allowing for further chemical modifications or conjugations for various research and diagnostic applications.
CAT: BRP-01336
CAS: 164394-19-8
Molecular Formula: C30H42N3O4P
Molecular Weight: 539.65
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InChIKey: HQKPKYLTHNVWSP-UHFFFAOYSA-N
CanonicalSMILES: N#CCCOP(OCCCCCCNC(=O)OCC1C=2C=CC=CC2C=3C=CC=CC31)N(C(C)C)C(C)C
IUPAC Name: (9H-fluoren-9-yl)methyl (6-(((2-cyanoethoxy)(diisopropylamino)phosphaneyl)oxy)hexyl)carbamate
InChI: InChI=1S/C30H42N3O4P/c1-23(2)33(24(3)4)38(37-21-13-18-31)36-20-12-6-5-11-19-32-30(34)35-22-29-27-16-9-7-14-25(27)26-15-8-10-17-28(26)29/h7-10,14-17,23-24,29H,5-6,11-13,19-22H2,1-4H3,(H,32,34)
Synonyms: 9-Oxa-2,11-diaza-10-phosphatridecanoic acid, 10-(2-cyanoethoxy)-12-methyl-11-(1-methylethyl)-, 9H-fluoren-9-ylmethyl ester; 9,11-Dioxa-2-aza-10-phosphatridecanoic acid, 10-[bis(1-methylethyl)amino]-13-cyano-, 9H-fluoren-9-ylmethyl ester; 9H-Fluoren-9-ylmethyl 10-(2-cyanoethoxy)-12-methyl-11-(1-methylethyl)-9-oxa-2,11-diaza-10-phosphatridecanoate

Fmoc-Amino-DMT C-7 CE phosphoramidite

Description: Fmoc-Amino-DMT C-7 CE phosphoramidite is a specialized compound utilized in oligonucleotide synthesis. It contains an Fmoc-protected amino group, a DMT group for 5' hydroxyl protection, and a C-7 spacer linked to a cyanoethyl (CE) phosphoramidite group. This compound enables controlled addition of amino functionalities to oligonucleotides, allowing for further chemical modifications or conjugations for various research and diagnostic applications.
CAT: BRP-01337
CAS: 2166602-99-7
Molecular Formula: C51H60N3O8P
Molecular Weight: 874.01
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InChIKey: AHZOYMSGLQGXPM-UHFFFAOYSA-N
CanonicalSMILES: N#CCCOP(OC(COCCCNC(=O)OCC1C=2C=CC=CC2C=3C=CC=CC31)COC(C=4C=CC=CC4)(C5=CC=C(OC)C=C5)C6=CC=C(OC)C=C6)N(C(C)C)C(C)C
IUPAC Name: (9H-fluoren-9-yl)methyl (3-(3-(bis(4-methoxyphenyl)(phenyl)methoxy)-2-(((2-cyanoethoxy)(diisopropylamino)phosphaneyl)oxy)propoxy)propyl)carbamate
InChI: InChI=1S/C51H60N3O8P/c1-37(2)54(38(3)4)63(61-33-14-30-52)62-44(34-58-32-15-31-53-50(55)59-36-49-47-20-12-10-18-45(47)46-19-11-13-21-48(46)49)35-60-51(39-16-8-7-9-17-39,40-22-26-42(56-5)27-23-40)41-24-28-43(57-6)29-25-41/h7-13,16-29,37-38,44,49H,14-15,31-36H2,1-6H3,(H,53,55)
Synonyms: 6,9-Dioxa-2,11-diaza-10-phosphatridecanoic acid, 8-[[bis(4-methoxyphenyl)phenylmethoxy]methyl]-10-(2-cyanoethoxy)-12-methyl-11-(1-methylethyl)-, 9H-fluoren-9-ylmethyl ester; 9H-Fluoren-9-ylmethyl 8-[[bis(4-methoxyphenyl)phenylmethoxy]methyl]-10-(2-cyanoethoxy)-12-methyl-11-(1-methylethyl)-6,9-dioxa-2,11-diaza-10-phosphatridecanoate

2,2'-Anhydro Uridine CED phosphoramidite

Description: 2,2'-Anhydro Uridine CED phosphoramidite is a specialized reagent used in oligonucleotide synthesis. This modification is attached to a phosphoramidite moiety with a cyanoethyl diisopropyl (CED) group, facilitating its incorporation into the growing oligonucleotide chain during solid-phase synthesis. This reagent enables the introduction of the 2,2'-anhydro uridine modification into synthetic oligonucleotides, allowing for the investigation of its effects on RNA structure and function.
CAT: BRP-01343
Molecular Formula: C39H45N4O8P
Molecular Weight: 728.77
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InChIKey: ZVSMFQYSVMROKY-SGXIJWRWSA-N
IUPAC Name: (2R,3R,3aS,9aR)-2-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-6-oxo-2,3,3a,9a-tetrahydro-6H-furo[2',3':4,5]oxazolo[3,2-a]pyrimidin-3-yl (2-cyanoethyl) diisopropylphosphoramidite
InChI: InChI=1S/C39H45N4O8P/c1-26(2)43(27(3)4)52(48-24-10-22-40)51-35-33(49-37-36(35)50-38-41-34(44)21-23-42(37)38)25-47-39(28-11-8-7-9-12-28,29-13-17-31(45-5)18-14-29)30-15-19-32(46-6)20-16-30/h7-9,11-21,23,26-27,33,35-37H,10,24-25H2,1-6H3/t33-,35-,36-,37-,52?/m1/s1
Synonyms: 6H-Furo[2',3':4,5]oxazolo[3,2-a]pyrimidine, 2-[[bis(4-methoxyphenyl)phenylmethoxy]methyl]-3-[[[bis(1-methylethyl)amino](2-cyanoethoxy)phosphino]oxy]-2,3,3a,9a-tetrahydro-6-oxo-, (2R,3R,3aS,9aR)-

Asymmetrical branching CED phosphoramidite

Description: Asymmetrical branching CED phosphoramidite is a chemical used to introduce branches into oligonucleotides during synthesis. It features an asymmetrical structure that enables the formation of complex, branched DNA or RNA sequences. This reagent is utilized in advanced molecular biology applications, such as the creation of multivalent probes, enhanced signal amplification assays, and the study of complex nucleic acid interactions.
CAT: BRP-01349
CAS: 345663-34-5
Molecular Formula: C38H49N2O8P
Molecular Weight: 692.78
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InChIKey: HYEDNLHCXFQSQY-UHFFFAOYSA-N
CanonicalSMILES: N#CCCOP(OC(COC(=O)CCC(=O)C)COC(C=1C=CC=CC1)(C2=CC=C(OC)C=C2)C3=CC=C(OC)C=C3)N(C(C)C)C(C)C
IUPAC Name: 3-(bis(4-methoxyphenyl)(phenyl)methoxy)-2-(((2-cyanoethoxy)(diisopropylamino)phosphaneyl)oxy)propyl 4-oxopentanoate
InChI: InChI=1S/C38H49N2O8P/c1-28(2)40(29(3)4)49(47-25-11-24-39)48-36(26-45-37(42)23-14-30(5)41)27-46-38(31-12-9-8-10-13-31,32-15-19-34(43-6)20-16-32)33-17-21-35(44-7)22-18-33/h8-10,12-13,15-22,28-29,36H,11,14,23,25-27H2,1-7H3
Synonyms: Pentanoic acid, 4-oxo-, 3-[bis(4-methoxyphenyl)phenylmethoxy]-2-[[[bis(1-methylethyl)amino](2-cyanoethoxy)phosphino]oxy]propyl ester; 3-[Bis(4-methoxyphenyl)phenylmethoxy]-2-[[[bis(1-methylethyl)amino](2-cyanoethoxy)phosphino]oxy]propyl 4-oxopentanoate

4-Triazolyl 2'-TBDMS Uridine CED phosphoramidite

Description: 4-Triazolyl Uridine CED phosphoramidite is a phosphoramidite derivative of uridine, featuring a 4-triazolyl modification at the 4-position and a tert-butyldimethylsilyl (TBDMS) protection group at the 2'-position. It is utilized in solid-phase oligonucleotide synthesis to introduce the 4-triazolyl modification, enabling the formation of triazole-linked nucleic acids. These modified nucleic acids can be used in various applications, including click chemistry-based conjugation strategies and the study of nucleic acid structure and function.
CAT: BRP-01356
CAS: 3033741-07-7
Molecular Formula: C47H62N7O8PSi
Molecular Weight: 912.10
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InChIKey: SDOHATSBOOYVAE-HEOXLOLOSA-N
CanonicalSMILES: N#CCCOP(OC1C(OC(N2C=CC(=NC2=O)N3N=CN=C3)C1O[Si](C)(C)C(C)(C)C)COC(C=4C=CC=CC4)(C5=CC=C(OC)C=C5)C6=CC=C(OC)C=C6)N(C(C)C)C(C)C
IUPAC Name: (2R,3R,4R,5R)-2-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-4-((tert-butyldimethylsilyl)oxy)-5-(2-oxo-4-(1H-1,2,4-triazol-1-yl)pyrimidin-1(2H)-yl)tetrahydrofuran-3-yl (2-cyanoethyl) diisopropylphosphoramidite
InChI: InChI=1S/C47H62N7O8PSi/c1-33(2)54(34(3)4)63(59-29-15-27-48)61-42-40(60-44(43(42)62-64(10,11)46(5,6)7)52-28-26-41(51-45(52)55)53-32-49-31-50-53)30-58-47(35-16-13-12-14-17-35,36-18-22-38(56-8)23-19-36)37-20-24-39(57-9)25-21-37/h12-14,16-26,28,31-34,40,42-44H,15,29-30H2,1-11H3/t40-,42-,43-,44-,63?/m1/s1
Synonyms: 2(1H)-Pyrimidinone, 1-[5-O-[bis(4-methoxyphenyl)phenylmethyl]-3-O-[[bis(1-methylethyl)amino](2-cyanoethoxy)phosphino]-2-O-[(1,1-dimethylethyl)dimethylsilyl]-β-D-ribofuranosyl]-4-(1H-1,2,4-triazol-1-yl)-; 4-Triazolyl Uridine CED phosphoramidite

Dabcyl CED phosphoramidite

Description: Dabcyl CED phosphoramidite is a phosphoramidite derivative used for introducing the Dabcyl moiety into oligonucleotide sequences during solid-phase synthesis. Dabcyl is a quencher molecule often employed in the design of molecular probes and assays, particularly for fluorescence-based detection methods. Its ability to quench fluorescence by energy transfer makes it useful for labeling nucleic acids and peptides for various biochemical and molecular biology applications, including fluorescence resonance energy transfer (FRET) assays, nucleic acid hybridization studies, and real-time PCR probes.
CAT: BRP-01357
CAS: 2128327-84-2
Molecular Formula: C51H63N6O7P
Molecular Weight: 903.06
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InChIKey: CFNGUZAXHBVWBU-UHFFFAOYSA-N
CanonicalSMILES: N#CCCOP(OC(COCCCNC(=O)C1=CC=C(N=NC2=CC=C(C=C2)N(C)C)C=C1)COC(C=3C=CC=CC3)(C4=CC=C(OC)C=C4)C5=CC=C(OC)C=C5)N(C(C)C)C(C)C
IUPAC Name: 1-(bis(4-methoxyphenyl)(phenyl)methoxy)-3-(3-(4-((4-(dimethylamino)phenyl)diazenyl)benzamido)propoxy)propan-2-yl (2-cyanoethyl) diisopropylphosphoramidite
InChI: InChI=1S/C51H63N6O7P/c1-38(2)57(39(3)4)65(63-35-12-32-52)64-49(36-61-34-13-33-53-50(58)40-16-22-44(23-17-40)54-55-45-24-26-46(27-25-45)56(5)6)37-62-51(41-14-10-9-11-15-41,42-18-28-47(59-7)29-19-42)43-20-30-48(60-8)31-21-43/h9-11,14-31,38-39,49H,12-13,33-37H2,1-8H3,(H,53,58)

DMT-5-FAM Phosphoramidite

Description: DMT-5-FAM Phosphoramidite is a phosphoramidite derivative used to incorporate 5-carboxyfluorescein (5-FAM) into oligonucleotides during solid-phase synthesis. It features a 5-FAM fluorophore and a dimethoxytrityl (DMT) protecting group. This reagent allows for the efficient synthesis of fluorescently labeled oligonucleotides, which are widely used in molecular biology applications such as fluorescence-based detection, quantitative PCR (qPCR), and various types of fluorescence resonance energy transfer (FRET) assays.
CAT: BRP-01361
CAS: 1799331-55-7
Molecular Formula: C68H78N3O13P
Molecular Weight: 1176.33
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InChIKey: SAAQCYSLOUHYEE-UHFFFAOYSA-N
CanonicalSMILES: N#CCCOP(OCC(COC(C=1C=CC=CC1)(C2=CC=C(OC)C=C2)C3=CC=C(OC)C=C3)CCCCNC(=O)C4=CC=C5C(=C4)C(=O)OC65C7=CC=C(OC(=O)C(C)(C)C)C=C7OC8=CC(OC(=O)C(C)(C)C)=CC=C86)N(C(C)C)C(C)C
IUPAC Name: 5-((6-(bis(4-methoxyphenyl)(phenyl)methoxy)-5-((((2-cyanoethoxy)(diisopropylamino)phosphaneyl)oxy)methyl)hexyl)carbamoyl)-3-oxo-3H-spiro[isobenzofuran-1,9'-xanthene]-3',6'-diyl bis(2,2-dimethylpropanoate)
InChI: InChI=1S/C68H78N3O13P/c1-44(2)71(45(3)4)85(79-38-18-36-69)80-43-46(42-78-67(48-20-14-13-15-21-48,49-23-27-51(76-11)28-24-49)50-25-29-52(77-12)30-26-50)19-16-17-37-70-61(72)47-22-33-56-55(39-47)62(73)84-68(56)57-34-31-53(81-63(74)65(5,6)7)40-59(57)83-60-41-54(32-35-58(60)68)82-64(75)66(8,9)10/h13-15,20-35,39-41,44-46H,16-19,37-38,42-43H2,1-12H3,(H,70,72)
Synonyms: Propanoic acid, 2,2-dimethyl-, 1,1'-[5-[7-[[bis(4-methoxyphenyl)phenylmethoxy]methyl]-10-[bis(1-methylethyl)amino]-13-cyano-1-oxo-9,11-dioxa-2-aza-10-phosphatridec-1-yl]-3-oxospiro[isobenzofuran-1(3H),9'-[9H]xanthene]-3',6'-diyl] ester; 1,1'-[5-[7-[[Bis(4-methoxyphenyl)phenylmethoxy]methyl]-10-[bis(1-methylethyl)amino]-13-cyano-1-oxo-9,11-dioxa-2-aza-10-phosphatridec-1-yl]-3-oxospiro[isobenzofuran-1(3H),9'-[9H]xanthene]-3',6'-diyl] bis(2,2-dimethylpropanoate)

Fluorescein CED phosphoramidite

Description: Fluorescein CED phosphoramidite is a phosphoramidite derivative of fluorescein, a fluorescent dye commonly used in molecular biology applications. This reagent is designed to be incorporated into oligonucleotides during solid-phase synthesis, allowing for the specific labeling of nucleic acids with fluorescein. Upon incorporation, the fluorescein moiety enables the detection and visualization of the labeled oligonucleotides using fluorescence-based techniques. This makes it valuable for various applications such as fluorescence in situ hybridization (FISH), fluorescence resonance energy transfer (FRET) assays, and real-time PCR (qPCR) where fluorescent labeling is required for detection and quantification.
CAT: BRP-01362
Molecular Formula: C67H77N4O13PS
Molecular Weight: 1209.39
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InChIKey: BZPUELAJXMHPLN-UHFFFAOYSA-N
CanonicalSMILES: N#CCCOP(N(C(C)C)C(C)C)OC(COC(C1=CC=CC=C1)(C2=CC=C(OC)C=C2)C3=CC=C(OC)C=C3)COCCCNC(NC4=CC=C(C56C(C=C7)=C(OC8=C5C=CC(OC(C(C)(C)C)=O)=C8)C=C7OC(C(C)(C)C)=O)C(C(O6)=O)=C4)=S
IUPAC Name: 5-(3-(3-(3-(bis(4-methoxyphenyl)(phenyl)methoxy)-2-(((2-cyanoethoxy)(diisopropylamino)phosphaneyl)oxy)propoxy)propyl)thioureido)-3-oxo-3H-spiro[isobenzofuran-1,9'-xanthene]-3',6'-diyl bis(2,2-dimethylpropanoate)
InChI: InChI=1S/C67H77N4O13PS/c1-43(2)71(44(3)4)85(79-37-16-34-68)84-53(42-78-66(45-18-14-13-15-19-45,46-20-25-49(75-11)26-21-46)47-22-27-50(76-12)28-23-47)41-77-36-17-35-69-63(86)70-48-24-31-55-54(38-48)60(72)83-67(55)56-32-29-51(80-61(73)64(5,6)7)39-58(56)82-59-40-52(30-33-57(59)67)81-62(74)65(8,9)10/h13-15,18-33,38-40,43-44,53H,16-17,35-37,41-42H2,1-12H3,(H2,69,70,86)

Tetrachloro-fluorescein cyclohexyl CED phosphoramidite

Description: Tetrachloro-fluorescein cyclohexyl CED phosphoramidite is a phosphoramidite derivative of tetrachloro-fluorescein cyclohexyl, a fluorescent dye. It is designed to be incorporated into oligonucleotides during solid-phase synthesis, enabling the specific labeling of nucleic acids with tetrachloro-fluorescein cyclohexyl. Once incorporated, this label allows for the detection and visualization of the labeled oligonucleotides using fluorescence-based techniques. It is a valuable tool in molecular biology applications such as fluorescence in situ hybridization (FISH), fluorescence resonance energy transfer (FRET) assays, and real-time PCR (qPCR), where specific fluorescent labeling is essential for detection and quantification.
CAT: BRP-01365
Molecular Formula: C69H74Cl4N3O13P
Molecular Weight: 1326.12
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InChIKey: SYZVSEPABCJTBW-UHFFFAOYSA-N
CanonicalSMILES: ClC1=CC2=C(C=C1OC(C(C)(C)C)=O)OC3=C(C=C(C(OC(C(C)(C)C)=O)=C3)Cl)C24C5=C(C(C(NC6CCC(COP(N(C(C)C)C(C)C)OCCC#N)(COC(C7=CC=CC=C7)(C8=CC=C(OC)C=C8)C9=CC=C(OC)C=C9)CC6)=O)=CC(Cl)=C5C(O4)=O)Cl
IUPAC Name: 6-((4-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-4-((((2-cyanoethoxy)(diisopropylamino)phosphaneyl)oxy)methyl)cyclohexyl)carbamoyl)-2',4,7,7'-tetrachloro-3-oxo-3H-spiro[isobenzofuran-1,9'-xanthene]-3',6'-diyl bis(2,2-dimethylpropanoate)
InChI: InChI=1S/C69H74Cl4N3O13P/c1-40(2)76(41(3)4)90(84-32-16-31-74)85-39-67(38-83-68(42-17-14-13-15-18-42,43-19-23-46(81-11)24-20-43)44-21-25-47(82-12)26-22-44)29-27-45(28-30-67)75-61(77)48-33-53(72)58-59(60(48)73)69(89-62(58)78)49-34-51(70)56(87-63(79)65(5,6)7)36-54(49)86-55-37-57(52(71)35-50(55)69)88-64(80)66(8,9)10/h13-15,17-26,33-37,40-41,45H,16,27-30,32,38-39H2,1-12H3,(H,75,77)
Synonyms: Propanoic acid, 2,2-dimethyl-, 6-[[[4-[[bis(4-methoxyphenyl)phenylmethoxy]methyl]-4-[[[[bis(1-methylethyl)amino](2-cyanoethoxy)phosphino]oxy]methyl]cyclohexyl]amino]carbonyl]-2',4,7,7'-tetrachloro-3-oxospiro[isobenzofuran-1(3H),9'-[9H]xanthene]-3',6'-diyl ester

Hexachloro-fluorescein cyclohexyl CED phosphoramidite

Description: Hexachloro-fluorescein cyclohexyl CED phosphoramidite is a phosphoramidite derivative of hexachloro-fluorescein cyclohexyl, a fluorescent dye. It is utilized in oligonucleotide synthesis to introduce hexachloro-fluorescein cyclohexyl labels into nucleic acid sequences. Once incorporated, this label enables the detection and visualization of the labeled oligonucleotides using fluorescence-based techniques. It is a valuable tool in molecular biology applications such as fluorescence in situ hybridization (FISH), fluorescence resonance energy transfer (FRET) assays, and real-time PCR (qPCR), where specific fluorescent labeling is essential for detection and quantification.
CAT: BRP-01366
Molecular Formula: C69H72Cl6N3O13P
Molecular Weight: 1395.01
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InChIKey: OXVDGSOEMHTDJI-UHFFFAOYSA-N
CanonicalSMILES: N#CCCOP(OCC1(COC(C=2C=CC=CC2)(C3=CC=C(OC)C=C3)C4=CC=C(OC)C=C4)CCC(NC(=O)C5=CC(Cl)=C6C(=O)OC7(C8=CC(Cl)=C(OC(=O)C(C)(C)C)C(Cl)=C8OC9=C(Cl)C(OC(=O)C(C)(C)C)=C(Cl)C=C97)C6=C5Cl)CC1)N(C(C)C)C(C)C
IUPAC Name: 6-((4-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-4-((((2-cyanoethoxy)(diisopropylamino)phosphaneyl)oxy)methyl)cyclohexyl)carbamoyl)-2',4,4',5',7,7'-hexachloro-3-oxo-3H-spiro[isobenzofuran-1,9'-xanthene]-3',6'-diyl bis(2,2-dimethylpropanoate)
InChI: InChI=1S/C69H72Cl6N3O13P/c1-38(2)78(39(3)4)92(86-32-16-31-76)87-37-67(36-85-68(40-17-14-13-15-18-40,41-19-23-44(83-11)24-20-41)42-21-25-45(84-12)26-22-42)29-27-43(28-30-67)77-61(79)46-33-49(70)52-53(54(46)73)69(91-62(52)80)47-34-50(71)59(89-63(81)65(5,6)7)55(74)57(47)88-58-48(69)35-51(72)60(56(58)75)90-64(82)66(8,9)10/h13-15,17-26,33-35,38-39,43H,16,27-30,32,36-37H2,1-12H3,(H,77,79)
Synonyms: Propanoic acid, 2,2-dimethyl-, 6-[[[4-[[bis(4-methoxyphenyl)phenylmethoxy]methyl]-4-[[[[bis(1-methylethyl)amino](2-cyanoethoxy)phosphino]oxy]methyl]cyclohexyl]amino]carbonyl]-2',4,4',5',7,7'-hexachloro-3-oxospiro[isobenzofuran-1(3H),9'-[9H]xanthene]-3',6'-diyl ester
* Only for research. Not suitable for any diagnostic or therapeutic use.

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