Nucleosides

2'-O-(2-Methoxyethyl)-5-methylcytidine hydrochloride

Description: It is used for oligonucleotide synthesis and biotechnological studies.

CAT: BRP-00767

Molecular Formula: C13H22ClN3O6

Molecular Weight: 351.78

Purity: ≥97% by HPLC

Appearance: White or off-white solid

Size	Price	Stock	Quantity
--	--	--

Inquiry

Storage: Store at 2-8 °C

InChIKey: YPFHLLIYUOCCOJ-YBZJUNAKSA-N

CanonicalSMILES: CC1=CN(C(=O)N=C1N)C2C(C(C(O2)CO)O)OCCOC.Cl

IUPAC Name: 4-amino-1-[(2R,3R,4R,5R)-4-hydroxy-5-(hydroxymethyl)-3-(2-methoxyethoxy)oxolan-2-yl]-5-methylpyrimidin-2-one;hydrochloride

InChI: InChI=1S/C13H21N3O6.ClH/c1-7-5-16(13(19)15-11(7)14)12-10(21-4-3-20-2)9(18)8(6-17)22-12;/h5,8-10,12,17-18H,3-4,6H2,1-2H3,(H2,14,15,19);1H/t8-,9-,10-,12-;/m1./s1

Synonyms: 5-Methyl-2'-methoxyethoxycytosine hydrochloride; Cytidine, 2'-O-(2-Methoxyethyl)-5-Methyl-, hydrochloride (1:1); 2'-O-MOE-5-Me-rC hydrochloride; 2'-MOE-5-Methycytidine hydrochloride; 5-Methyl-2'-O-methoxyethyl-cytidine hydrochloride

Related CAS: 244105-55-3 (free base)

5'-O-DMT-5-Hydroxyethyl-dU

Description: 5'-O-DMT-5-Hydroxyethyl-dU is a modified form of deoxyuridine (dU) featuring a 5'-O-DMT (dimethoxytrityl) protecting group and a hydroxyethyl moiety at the 5 position of the uracil base. This modification introduces hydrophilicity and alters the base pairing properties of the nucleotide, making it useful in various biochemical applications, including DNA synthesis and structural studies.

CAT: BRP-00768

CAS: 1411974-64-5

Molecular Formula: C32H34N2O8

Molecular Weight: 574.63

Size	Price	Stock	Quantity
--	--	--

Inquiry

Density: 1.297±0.06 g/cm3

InChIKey: KCPHUOHHZQNELQ-ZGIBFIJWSA-N

CanonicalSMILES: O=C1NC(=O)N(C=C1CCO)C2OC(COC(C=3C=CC=CC3)(C4=CC=C(OC)C=C4)C5=CC=C(OC)C=C5)C(O)C2

IUPAC Name: 1-((2R,4S,5R)-5-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-4-hydroxytetrahydrofuran-2-yl)-5-(2-hydroxyethyl)pyrimidine-2,4(1H,3H)-dione

InChI: InChI=1S/C32H34N2O8/c1-39-25-12-8-23(9-13-25)32(22-6-4-3-5-7-22,24-10-14-26(40-2)15-11-24)41-20-28-27(36)18-29(42-28)34-19-21(16-17-35)30(37)33-31(34)38/h3-15,19,27-29,35-36H,16-18,20H2,1-2H3,(H,33,37,38)/t27-,28+,29+/m0/s1

Synonyms: 5'-O-DMT-5-Hydroxyethyl-2'-deoxyuridine; 5'-O-DMT-2'-Deoxy-5-(hydroxyethyl)uridine; 5'-O-[Bis(4-methoxyphenyl)phenylmethyl]-2'-deoxy-5-(2-hydroxyethyl)uridine

5'-O-DMT-2'-O-TBDMS-N2-ibu-L-rG

Description: 5'-O-DMT-2'-O-TBDMS-N2-ibu-L-rG is a guanosine derivative used in RNA synthesis, with a 5'-O-DMT protecting group, a TBDMS (tert-butyldimethylsilyl) group at the 2' position, and an N2-isobutyryl-L modifier at the guanine base. This modification enhances stability and controlled reactivity during oligonucleotide assembly, making it suitable for RNA research and therapeutic development.

CAT: BRP-00769

CAS: 679809-77-9

Molecular Formula: C41H51N5O8Si

Molecular Weight: 769.97

Purity: ≥97% by HPLC

Size	Price	Stock	Quantity
--	--	--

Inquiry

Density: 1.25±0.1 g/cm3

InChIKey: JMCNKJFOIJGYRG-XECBKSLKSA-N

CanonicalSMILES: CC(C)C(=O)NC1=NC2=C(C(=O)N1)N=CN2C3C(C(C(O3)COC(C4=CC=CC=C4)(C5=CC=C(C=C5)OC)C6=CC=C(C=C6)OC)O)O[Si](C)(C)C(C)(C)C

IUPAC Name: N-[9-[(2S,3S,4S,5S)-5-[[bis(4-methoxyphenyl)-phenylmethoxy]methyl]-3-[tert-butyl(dimethyl)silyl]oxy-4-hydroxyoxolan-2-yl]-6-oxo-1H-purin-2-yl]-2-methylpropanamide

InChI: InChI=1S/C41H51N5O8Si/c1-25(2)36(48)44-39-43-35-32(37(49)45-39)42-24-46(35)38-34(54-55(8,9)40(3,4)5)33(47)31(53-38)23-52-41(26-13-11-10-12-14-26,27-15-19-29(50-6)20-16-27)28-17-21-30(51-7)22-18-28/h10-22,24-25,31,33-34,38,47H,23H2,1-9H3,(H2,43,44,45,48,49)/t31-,33-,34-,38-/m0/s1

Synonyms: 5'-O-DMT-2'-O-(tertbutyldimethylsilyl)-N2-isobutyryl-L-Guanosine; N-[9-[5-O-[Bis(4-methoxyphenyl)phenylmethyl]-2-O-[(1,1-dimethylethyl)dimethylsilyl]-β-L-ribofuranosyl]-6,9-dihydro-6-oxo-1H-purin-2-yl]-2-methylpropanamide

N6-Benzoyl-2',3'-di-O-acetyladenosine

Description: N6-Benzoyl-2’,3’-di-O-acetyladenosine is a modified form of adenosine featuring a benzoyl group at the N6 position and di-O-acetyl groups at the 2' and 3' positions of the ribose sugar. These modifications provide stability and alter the chemical properties of adenosine, making it useful in various biochemical applications, including RNA synthesis and modification studies.

CAT: BRP-00770

CAS: 69293-36-3

Molecular Formula: C21H21N5O7

Molecular Weight: 455.43

Purity: ≥95%

Appearance: White to off-white powder

Size	Price	Stock	Quantity
--	--	--

Inquiry

Storage: Store at 2-8 °C

Density: 1.55±0.1 g/cm3

InChIKey: FGYJKVXTRQIWTE-VGKBRBPRSA-N

CanonicalSMILES: CC(=O)OC1C(OC(C1OC(=O)C)N2C=NC3=C(N=CN=C32)NC(=O)C4=CC=CC=C4)CO

IUPAC Name: [(2R,3R,4R,5R)-4-acetyloxy-5-(6-benzamidopurin-9-yl)-2-(hydroxymethyl)oxolan-3-yl] acetate

InChI: InChI=1S/C21H21N5O7/c1-11(28)31-16-14(8-27)33-21(17(16)32-12(2)29)26-10-24-15-18(22-9-23-19(15)26)25-20(30)13-6-4-3-5-7-13/h3-7,9-10,14,16-17,21,27H,8H2,1-2H3,(H,22,23,25,30)/t14-,16-,17-,21-/m1/s1

Synonyms: Adenosine, N-benzoyl-, 2',3'-diacetate; 2',3'-di-O-Acetyl-N6-Benzoyl-Adenosine; N6-Bz-2',3'-Acetyl-Adenosine; N6-benzoyl-2',3'-Acetyl-Adenosine; (2R,3R,4R,5R)-2-(6-benzamido-9H-purin-9-yl)-5-(hydroxymethyl)tetrahydrofuran-3,4-diyl diacetate; 2',3'-diAc-A(Bz); N6-benzoyl-2',3'-diacetyl-adenosine

(E)-N'-(1-Benzyl-9-((2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-6-oxo-6,9-dihydro-1H-purin-2-yl)-N,N-dimethylformimidamide

Description: (E)-N'-(1-Benzyl-9-((2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-6-oxo-6,9-dihydro-1H-purin-2-yl)-N,N-dimethylformimidamide is a chemical compound used in organic synthesis and medicinal chemistry. It is often utilized as a precursor or intermediate in the synthesis of nucleoside analogs or other bioactive compounds.

CAT: BRP-00795

Molecular Formula: C20H24N6O5

Molecular Weight: 428.44

Purity: 98%

Size	Price	Stock	Quantity
--	--	--

Inquiry

InChIKey: ALGXQQKQSPSJBB-DJWODFLFSA-N

InChI: InChI=1S/C20H24N6O5/c1-24(2)10-22-20-23-17-14(18(30)25(20)8-12-6-4-3-5-7-12)21-11-26(17)19-16(29)15(28)13(9-27)31-19/h3-7,10-11,13,15-16,19,27-29H,8-9H2,1-2H3/b22-10+/t13-,15-,16-,19-/m1/s1

5,8-Dihydro-N,N,5-trimethyl-8-β-D-ribofuranosylpyrrolo[2',3':4,5]pyrrolo[2,3-d]pyrimidin-4-amine

Description: 5,8-Dihydro-N,N,5-trimethyl-8-β-D-ribofuranosylpyrrolo[2',3':4,5]pyrrolo[2,3-d]pyrimidin-4-amine is a chemical compound with potential biological activity. It is often studied for its potential pharmacological properties or as a building block in medicinal chemistry for the synthesis of nucleoside analogs.

CAT: BRP-00796

CAS: 2180983-51-9

Molecular Formula: C16H21N5O4

Molecular Weight: 347.37

Purity: 98%

Size	Price	Stock	Quantity
--	--	--

Inquiry

Density: 1.62±0.1 g/cm3

Boiling Point: 588.6±50.0 °C at 760 mmHg

InChIKey: GIPKNLNHAZHJMS-RVXWVPLUSA-N

CanonicalSMILES: CN1C=CC2=C1C3=C(N2C4C(C(C(O4)CO)O)O)N=CN=C3N(C)C

IUPAC Name: (2R,3R,4S,5R)-2-[12-(dimethylamino)-3-methyl-3,7,9,11-tetrazatricyclo[6.4.0.02,6]dodeca-1(8),2(6),4,9,11-pentaen-7-yl]-5-(hydroxymethyl)oxolane-3,4-diol

InChI: InChI=1S/C16H21N5O4/c1-19(2)14-10-11-8(4-5-20(11)3)21(15(10)18-7-17-14)16-13(24)12(23)9(6-22)25-16/h4-5,7,9,12-13,16,22-24H,6H2,1-3H3/t9-,12-,13-,16-/m1/s1

Synonyms: Pyrrolo[2',3':4,5]pyrrolo[2,3-d]pyrimidin-4-amine, 5,8-dihydro-N,N,5-trimethyl-8-β-D-ribofuranosyl-; (2R,3R,4S,5R)-2-(4-(Dimethylamino)-5-methylpyrrolo[2',3':4,5]pyrrolo[2,3-d]pyrimidin-8(5H)-yl)-5-(hydroxymethyl)tetrahydrofuran-3,4-diol

5-O-DMT-N2-Dimethylformamide-2-O-methylguanosine

Description: 5-O-DMT-N2-Dimethylformamide-2-O-methylguanosine is a modified nucleoside compound commonly used in RNA synthesis and modification studies. It is often employed as a building block for the synthesis of RNA molecules with specific modifications for various biological and research purposes.

CAT: BRP-00797

CAS: 1858223-91-2

Molecular Formula: C35H38N6O7

Molecular Weight: 654.71

Purity: 97%

Appearance: White powder

Size	Price	Stock	Quantity
--	--	--

Inquiry

Storage: Store at 2-8 °C, Keep in a dark and dry place

Density: 1.33±0.1 g/cm3

Boiling Point: 848.7±75.0 °C at 760 mmHg

InChIKey: SBJHBQZDABMKCF-JHZZHVAFSA-N

CanonicalSMILES: CN(C)C=NC1=NC2=C(C(=O)N1)N=CN2C3C(C(C(O3)COC(C4=CC=CC=C4)(C5=CC=C(C=C5)OC)C6=CC=C(C=C6)OC)O)OC

IUPAC Name: N'-[9-[(2R,3R,4R,5R)-5-[[bis(4-methoxyphenyl)-phenylmethoxy]methyl]-4-hydroxy-3-methoxyoxolan-2-yl]-6-oxo-1H-purin-2-yl]-N,N-dimethylmethanimidamide

InChI: InChI=1S/C35H38N6O7/c1-40(2)20-37-34-38-31-28(32(43)39-34)36-21-41(31)33-30(46-5)29(42)27(48-33)19-47-35(22-9-7-6-8-10-22,23-11-15-25(44-3)16-12-23)24-13-17-26(45-4)18-14-24/h6-18,20-21,27,29-30,33,42H,19H2,1-5H3,(H,38,39,43)/t27-,29-,30-,33-/m1/s1

Synonyms: N'-(9-((2R,3R,4R,5R)-5-((Bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-4-hydroxy-3-methoxytetrahydrofuran-2-yl)-6-oxo-6,9-dihydro-1H-purin-2-yl)-N,N-dimethylformimidamide; 5'-O-DMT-N2-DMF-2'-O-methylguanosine; N2-dmf-DMT-2'-OMe-Gr; N2-dimethylformamidine-5'-O-(4,4'-dimethoxytrityl)-2'-O-methyl-Guanosine

(E)-N2-Dimethylformamide-2-O-methylguanosine

Description: (E)-N2-Dimethylformamide-2-O-methylguanosine is a modified nucleoside compound used in RNA synthesis and modification studies. It is commonly employed as a building block for the synthesis of RNA molecules with specific modifications, allowing researchers to investigate RNA structure, function, and interactions.

CAT: BRP-00798

CAS: 1951424-87-5

Molecular Formula: C14H20N6O5

Molecular Weight: 352.35

Purity: 98%

Size	Price	Stock	Quantity
--	--	--

Inquiry

Density: 1.63±0.1 g/cm3

Boiling Point: 672.2±65.0 °C at 760 mmHg

InChIKey: KDQQTCFKBCWYFL-GTACIXLRSA-N

CanonicalSMILES: CN(C)C=NC1=NC2=C(C(=O)N1)N=CN2C3C(C(C(O3)CO)O)OC

IUPAC Name: (E)-N'-[9-[(2R,3R,4R,5R)-4-hydroxy-5-(hydroxymethyl)-3-methoxyoxolan-2-yl]-6-oxo-1H-purin-2-yl]-N,N-dimethylmethanimidamide

InChI: InChI=1S/C14H20N6O5/c1-19(2)5-16-14-17-11-8(12(23)18-14)15-6-20(11)13-10(24-3)9(22)7(4-21)25-13/h5-7,9-10,13,21-22H,4H2,1-3H3,(H,17,18,23)/b16-5+/t7-,9-,10-,13-/m1/s1

Synonyms: (E)-N-[(Dimethylamino)methylene]-2'-O-methylguanosine; (E)-N'-(9-((2R,3R,4R,5R)-4-Hydroxy-5-(hydroxymethyl)-3-methoxytetrahydrofuran-2-yl)-6-oxo-6,9-dihydro-1H-purin-2-yl)-N,N-dimethylformimidamide

Related CAS: 183737-04-4 (N-[(Dimethylamino)methylene]-2'-O-methylguanosine)

[N(E)]-N-[(Dimethylamino)methylene]guanosine

Description: [N(E)]-N-[(Dimethylamino)methylene]guanosine is a modified nucleoside compound commonly utilized in biochemical research, particularly in RNA studies. This modification is often used to investigate RNA structure, function, and interactions, providing valuable insights into biological processes such as RNA folding, RNA-protein interactions, and RNA catalysis.

CAT: BRP-00799

CAS: 1055407-32-3

Molecular Formula: C13H18N6O5

Molecular Weight: 338.32

Purity: 98%

Size	Price	Stock	Quantity
--	--	--

Inquiry

Density: 1.77±0.1 g/cm3

Boiling Point: 708.5±70.0 °C at 760 mmHg

InChIKey: WDAVDBAMSKZBEN-PZYHSTABSA-N

CanonicalSMILES: CN(C)C=NC1=NC2=C(C(=O)N1)N=CN2C3C(C(C(O3)CO)O)O

IUPAC Name: (E)-N'-[9-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-6-oxo-1H-purin-2-yl]-N,N-dimethylmethanimidamide

InChI: InChI=1S/C13H18N6O5/c1-18(2)4-15-13-16-10-7(11(23)17-13)14-5-19(10)12-9(22)8(21)6(3-20)24-12/h4-6,8-9,12,20-22H,3H2,1-2H3,(H,16,17,23)/b15-4+/t6-,8-,9-,12-/m1/s1

Synonyms: (E)-N'-(9-((2R,3R,4S,5R)-3,4-Dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-6-oxo-6,9-dihydro-3H-purin-2-yl)-N,N-dimethylformimidamide; Guanosine, N-[(dimethylamino)methylene]-, [N(E)]-; (E)-N2-DMF-rG; N-dimethylaminomethylene guanosine

Related CAS: 17331-16-7 (N-[(Dimethylamino)methylene]guanosine)

2'-O-TBDMS-N2-DMF-rG

Description: 2'-O-TBDMS-N2-DMF-rG is a modified nucleoside commonly employed in RNA synthesis and modification studies. It contains a guanosine base with modifications at the 2'-position (TBDMS) and N2 position (DMF). The TBDMS group protects the 2'-hydroxyl group, while the DMF group is attached to the N2 position. This modification allows researchers to introduce specific functionalities into RNA molecules for various research purposes, such as structural studies, RNA-protein interactions, or RNA labeling experiments, providing valuable insights into RNA biology and function.

CAT: BRP-00800

CAS: 126922-63-2

Molecular Formula: C19H32N6O5Si

Molecular Weight: 452.58

Purity: 98%

Size	Price	Stock	Quantity
--	--	--

Inquiry

Density: 1.34±0.1 g/cm3

InChIKey: ILIKLOCTYDXXNJ-LSCFUAHRSA-N

CanonicalSMILES: CC(C)(C)[Si](C)(C)OC1C(C(OC1N2C=NC3=C2N=C(NC3=O)N=CN(C)C)CO)O

IUPAC Name: N'-[9-[(2R,3R,4R,5R)-3-[tert-butyl(dimethyl)silyl]oxy-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-6-oxo-1H-purin-2-yl]-N,N-dimethylmethanimidamide

InChI: InChI=1S/C19H32N6O5Si/c1-19(2,3)31(6,7)30-14-13(27)11(8-26)29-17(14)25-10-20-12-15(25)22-18(23-16(12)28)21-9-24(4)5/h9-11,13-14,17,26-27H,8H2,1-7H3,(H,22,23,28)/t11-,13-,14-,17-/m1/s1

Synonyms: Guanosine, N-[(dimethylamino)methylene]-2'-O-[(1,1-dimethylethyl)dimethylsilyl]-; N-[(Dimethylamino)methylene]-2'-O-[(1,1-dimethylethyl)dimethylsilyl]guanosine; N'-(9-((2R,3R,4R,5R)-3-((tert-Butyldimethylsilyl)oxy)-4-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-6-oxo-6,9-dihydro-1H-purin-2-yl)-N,N-dimethylformimidamide

5-Bromotubercidin

Description: 5-Bromotubercidin is a chemical compound commonly utilized in biochemical research and drug development. It belongs to the class of tubercidin analogs and is known for its inhibitory effects on various enzymes, including kinases.

CAT: BRP-00801

CAS: 21193-80-6

Molecular Formula: C11H13BrN4O4

Molecular Weight: 345.15

Purity: 97%

Appearance: White to off-white solid

Size	Price	Stock	Quantity
--	--	--

Inquiry

Storage: Store at 2-8 °C, protect from light

Density: 2.26±0.1 g/cm3

Melting Point: 232 °C

Boiling Point: 686.9±55.0 °C at 760 mmHg

InChIKey: ZWTPRQXZXQEKFT-IOSLPCCCSA-N

Solubility: Soluble in DMSO (Slightly), Methanol (Slightly)

CanonicalSMILES: C1=C(C2=C(N=CN=C2N1C3C(C(C(O3)CO)O)O)N)Br

IUPAC Name: (2R,3R,4S,5R)-2-(4-amino-5-bromopyrrolo[2,3-d]pyrimidin-7-yl)-5-(hydroxymethyl)oxolane-3,4-diol

InChI: InChI=1S/C11H13BrN4O4/c12-4-1-16(10-6(4)9(13)14-3-15-10)11-8(19)7(18)5(2-17)20-11/h1,3,5,7-8,11,17-19H,2H2,(H2,13,14,15)/t5-,7-,8-,11-/m1/s1

Synonyms: (2R,3R,4S,5R)-2-(4-Amino-5-bromo-7H-pyrrolo[2,3-d]pyrimidin-7-yl)-5-(hydroxymethyl)tetrahydrofuran-3,4-diol; Bromotubercidin; 5-Bromo-7-β-D-ribofuranosyl-7H-pyrrolo[2,3-d]pyrimidin-4-amine; NSC103802

O2',O3',O5'-Tribenzoyl-5-methyl-2-thiouridine

Description: O2',O3',O5'-Tribenzoyl-5-methyl-2-thiouridine is a modified nucleoside compound often used in RNA research and modification studies. It contains a uridine base with modifications at the 2nd position (thio), and the 2', 3', and 5' hydroxyl groups are tribenzoylated. This modification is utilized to study RNA structure, function, and interactions, providing insights into RNA biology and potential therapeutic applications.

CAT: BRP-00802

CAS: 75921-08-3

Molecular Formula: C31H26N2O8S

Molecular Weight: 586.61

Purity: 98%

Size	Price	Stock	Quantity
--	--	--

Inquiry

Density: 1.43±0.1 g/cm3

InChIKey: JEAZFXFXZLAZLW-DLGLWYJGSA-N

CanonicalSMILES: CC1=CN(C(=S)NC1=O)C2C(C(C(O2)COC(=O)C3=CC=CC=C3)OC(=O)C4=CC=CC=C4)OC(=O)C5=CC=CC=C5

IUPAC Name: [(2R,3R,4R,5R)-3,4-dibenzoyloxy-5-(5-methyl-4-oxo-2-sulfanylidenepyrimidin-1-yl)oxolan-2-yl]methyl benzoate

InChI: InChI=1S/C31H26N2O8S/c1-19-17-33(31(42)32-26(19)34)27-25(41-30(37)22-15-9-4-10-16-22)24(40-29(36)21-13-7-3-8-14-21)23(39-27)18-38-28(35)20-11-5-2-6-12-20/h2-17,23-25,27H,18H2,1H3,(H,32,34,42)/t23-,24-,25-,27-/m1/s1

Synonyms: (2R,3R,4R,5R)-2-((Benzoyloxy)methyl)-5-(5-methyl-4-oxo-2-thioxo-3,4-dihydropyrimidin-1(2H)-yl)tetrahydrofuran-3,4-diyl dibenzoate; Uridine, 5-methyl-2-thio-, 2',3',5'-tribenzoate

2',3'-O-Isopropylidenecytidine sulfate

Description: 2',3'-O-Isopropylidenecytidine sulfate is a modified nucleoside compound frequently employed in RNA synthesis and modification studies. It contains a cytidine base with protection at the 2' and 3' hydroxyl groups by isopropylidene and is in the form of a sulfate salt.

CAT: BRP-00803

CAS: 1955522-00-5

Molecular Formula: C12H19N3O9S

Molecular Weight: 381.36

Purity: 98%

Size	Price	Stock	Quantity
--	--	--

Inquiry

InChIKey: WEIXBFRDOMNWIS-RQDZQORCSA-N

CanonicalSMILES: CC1(OC2C(OC(C2O1)N3C=CC(=NC3=O)N)CO)C.OS(=O)(=O)O

IUPAC Name: 1-[(3aR,4R,6R,6aR)-6-(hydroxymethyl)-2,2-dimethyl-3a,4,6,6a-tetrahydrofuro[3,4-d][1,3]dioxol-4-yl]-4-aminopyrimidin-2-one;sulfuric acid

InChI: InChI=1S/C12H17N3O5.H2O4S/c1-12(2)19-8-6(5-16)18-10(9(8)20-12)15-4-3-7(13)14-11(15)17;1-5(2,3)4/h3-4,6,8-10,16H,5H2,1-2H3,(H2,13,14,17);(H2,1,2,3,4)/t6-,8-,9-,10-;/m1./s1

Synonyms: 4-Amino-1-((3aR,4R,6R,6aR)-6-(hydroxymethyl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)pyrimidin-2(1H)-one sulfate; 2',3'-Isopropylidenecytidine sulfate; 2',3'-O-(1-Methylethylidene)cytidine sulfate

Related CAS: 362-42-5 (free base)

1-(β-D-lyxofuranosyl)uracil

Description: 1-(β-D-lyxofuranosyl)uracil is a nucleoside compound commonly used in nucleic acid research and drug development. This modified nucleoside is employed in the study of nucleic acid structure and function, and can be used as an analog in the synthesis of oligonucleotides. Additionally, it has potential applications in the development of antiviral and anticancer therapeutics by mimicking natural nucleosides and interfering with nucleic acid metabolism.

CAT: BRP-00804

CAS: 4348-61-2

Molecular Formula: C9H12N2O6

Molecular Weight: 244.20

Purity: 98%

Size	Price	Stock	Quantity
--	--	--

Inquiry

Density: 1.674±0.06 g/cm3 (Predicted)

Melting Point: 203-204 °C

InChIKey: DRTQHJPVMGBUCF-YDKYIBAVSA-N

CanonicalSMILES: C1=CN(C(=O)NC1=O)C2C(C(C(O2)CO)O)O

IUPAC Name: 1-[(2R,3S,4R,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]pyrimidine-2,4-dione

InChI: InChI=1S/C9H12N2O6/c12-3-4-6(14)7(15)8(17-4)11-2-1-5(13)10-9(11)16/h1-2,4,6-8,12,14-15H,3H2,(H,10,13,16)/t4-,6+,7+,8-/m1/s1

Synonyms: 1-((2R,3S,4R,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)pyrimidine-2,4(1H,3H)-dione; 1-β-D-lyxofuranosyl-uracil; 2,4(1H,3H)-Pyrimidinedione, 1-β-D-lyxofuranosyl-

(E)-Ethyl 3-(1-((2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-5-yl)acrylate

Description: (E)-Ethyl 3-(1-((2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-5-yl)acrylate is a modified nucleoside derivative used in biochemical and pharmaceutical research. The modifications enhance its utility in studying nucleic acid interactions and functions, and it can serve as an intermediate in the synthesis of nucleoside analogs. These analogs have potential therapeutic applications, particularly in antiviral and anticancer treatments, by interfering with nucleic acid metabolism and replication processes.

CAT: BRP-00805

CAS: 123881-85-6

Molecular Formula: C14H18N2O8

Molecular Weight: 342.30

Purity: 98%

Size	Price	Stock	Quantity
--	--	--

Inquiry

Storage: Store at 2-8 °C

Density: 1.583±0.06 g/cm3

InChIKey: ATSFSUUXRHMGQU-BGFIHSBQSA-N

CanonicalSMILES: CCOC(=O)C=CC1=CN(C(=O)NC1=O)C2C(C(C(O2)CO)O)O

IUPAC Name: ethyl (E)-3-[1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-2,4-dioxopyrimidin-5-yl]prop-2-enoate

InChI: InChI=1S/C14H18N2O8/c1-2-23-9(18)4-3-7-5-16(14(22)15-12(7)21)13-11(20)10(19)8(6-17)24-13/h3-5,8,10-11,13,17,19-20H,2,6H2,1H3,(H,15,21,22)/b4-3+/t8-,10-,11-,13-/m1/s1

Synonyms: 2-Propenoic acid, 3-[1,2,3,4-tetrahydro-2,4-dioxo-1-β-D-ribofuranosyl-5-pyrimidinyl]-, ethyl ester, (E)-

6-Fluoro-3,4-dihydro-3-oxo-4-(2,3,5-tri-O-acetyl-β-D-ribofuranosyl)pyrazinecarboxamide

Description: 6-Fluoro-3,4-dihydro-3-oxo-4-(2,3,5-tri-O-acetyl-β-D-ribofuranosyl)pyrazinecarboxamide is a modified nucleoside analog used in biochemical research and pharmaceutical development. The modifications enhance its stability and facilitate its incorporation into nucleic acids. It is often utilized in the synthesis of nucleoside analogs for studying nucleic acid interactions, function, and potential therapeutic applications, particularly in the development of antiviral and anticancer agents.

CAT: BRP-00807

CAS: 499785-96-5

Molecular Formula: C16H18FN3O9

Molecular Weight: 415.33

Purity: 98%

Size	Price	Stock	Quantity
--	--	--

Inquiry

Density: 1.61±0.1 g/cm3

Boiling Point: 524.4±60.0 °C at 760 mmHg

InChIKey: IVDSFFUXGZDUGN-RVXWVPLUSA-N

CanonicalSMILES: CC(=O)OCC1C(C(C(O1)N2C=C(N=C(C2=O)C(=O)N)F)OC(=O)C)OC(=O)C

IUPAC Name: [(2R,3R,4R,5R)-3,4-diacetyloxy-5-(3-carbamoyl-5-fluoro-2-oxopyrazin-1-yl)oxolan-2-yl]methyl acetate

InChI: InChI=1S/C16H18FN3O9/c1-6(21)26-5-9-12(27-7(2)22)13(28-8(3)23)16(29-9)20-4-10(17)19-11(14(18)24)15(20)25/h4,9,12-13,16H,5H2,1-3H3,(H2,18,24)/t9-,12-,13-,16-/m1/s1

Synonyms: Pyrazinecarboxamide, 6-fluoro-3,4-dihydro-3-oxo-4-(2,3,5-tri-O-acetyl-β-D-ribofuranosyl)-; Acetic acid (2R,3R,4R,5R)-3,4-diacetoxy-5-(3-carbamoyl-5-fluoro-2-oxo-2H-pyrazin-1-yl)-tetrahydro-furan-2-ylmethyl ester; (2R,3R,4R,5R)-2-(Acetoxymethyl)-5-(3-carbamoyl-5-fluoro-2-oxopyrazin-1(2H)-yl)tetrahydrofuran-3,4-diyl diacetate

2-O-Ethyl-2'-O-methyluridine

Description: 2-O-Ethyl-2'-O-methyluridine is a modified nucleoside used in biochemical research, particularly in the study of RNA synthesis and modification. These modifications increase the stability and resistance to enzymatic degradation of the nucleoside, making it useful in the development of therapeutic oligonucleotides and the study of RNA structure and function.

CAT: BRP-00808

CAS: 1352173-49-9

Molecular Formula: C12H18N2O6

Molecular Weight: 286.28

Purity: 98%

Size	Price	Stock	Quantity
--	--	--

Inquiry

Density: 1.47±0.1 g/cm3

Boiling Point: 466.2±55.0 °C at 760 mmHg

InChIKey: NZNRDRCBHUXJKX-QCNRFFRDSA-N

CanonicalSMILES: CCOC1=NC(=O)C=CN1C2C(C(C(O2)CO)O)OC

IUPAC Name: 2-ethoxy-1-[(2R,3R,4R,5R)-4-hydroxy-5-(hydroxymethyl)-3-methoxyoxolan-2-yl]pyrimidin-4-one

InChI: InChI=1S/C12H18N2O6/c1-3-19-12-13-8(16)4-5-14(12)11-10(18-2)9(17)7(6-15)20-11/h4-5,7,9-11,15,17H,3,6H2,1-2H3/t7-,9-,10-,11-/m1/s1

Synonyms: 2'-O-Methyl-2-O-ethyluridine; 2-Ethoxy-1-((2R,3R,4R,5R)-4-hydroxy-5-(hydroxymethyl)-3-methoxytetrahydrofuran-2-yl)pyrimidin-4(1H)-one

S-(5')-Adenosyl-3-thiopropylamine

Description: S-(5')-Adenosyl-3-thiopropylamine is a modified nucleoside compound used in biochemical research, particularly in the study of enzyme mechanisms and metabolic pathways. This compound consists of an adenosine moiety linked to a 3-thiopropylamine group via a sulfur atom at the 5' position. It serves as a cofactor or substrate analog in various enzymatic reactions, providing insights into the role of sulfur-containing nucleosides in biological processes and potential therapeutic applications.

CAT: BRP-00810

CAS: 53186-57-5

Molecular Formula: C13H20N6O3S

Molecular Weight: 340.40

Purity: 98%

Size	Price	Stock	Quantity
--	--	--

Inquiry

Density: 1.78±0.1 g/cm3

Boiling Point: 683.7±65.0 °C at 760 mmHg

InChIKey: FUSRAALGPJJIRO-QYVSTXNMSA-N

CanonicalSMILES: C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)CSCCCN)O)O)N

IUPAC Name: (2S,3S,4R,5R)-2-(3-aminopropylsulfanylmethyl)-5-(6-aminopurin-9-yl)oxolane-3,4-diol

InChI: InChI=1S/C13H20N6O3S/c14-2-1-3-23-4-7-9(20)10(21)13(22-7)19-6-18-8-11(15)16-5-17-12(8)19/h5-7,9-10,13,20-21H,1-4,14H2,(H2,15,16,17)/t7-,9-,10-,13-/m1/s1

Synonyms: S-Adenosyl-3-thiopropylamine; 5'-S-(3-Aminopropyl)-5'-thioadenosine; 5''-(Aminopropylthio)-5''-deoxy-adenosine; (2R,3R,4S,5S)-2-(6-amino-9H-purin-9-yl)-5-((3-aminopropylthio)methyl)tetrahydrofuran-3,4-diol

Related CAS: 99019-00-8 (sulfate)

N4-Ac-2'-O-4'-C-Locked-Cr

Description: N4-Ac-2'-O-4'-C-Locked-Cr is a modified nucleoside used in oligonucleotide synthesis. It consists of an acetyl group (Ac) at the N4 position of the cytosine, a 2'-O modification, and a 4'-carbon locked cytosine (Locked-Cr). This modification is designed to stabilize the oligonucleotide structure and alter its properties for specific applications in nucleic acid research and biotechnology.

CAT: BRP-00986

CAS: 391199-75-0

Molecular Formula: C12H15N3O6

Molecular Weight: 297.27

Size	Price	Stock	Quantity
--	--	--

Inquiry

Density: 1.77±0.1 g/cm3

Melting Point: 223-225 °C (dec.)

InChIKey: DLDUBZSJKKUTMP-KLBPJQLPSA-N

CanonicalSMILES: CC(=O)NC1=NC(=O)N(C=C1)C2C3C(C(O2)(CO3)CO)O

IUPAC Name: N-[1-[(1S,3R,4R,7S)-7-hydroxy-1-(hydroxymethyl)-2,5-dioxabicyclo[2.2.1]heptan-3-yl]-2-oxopyrimidin-4-yl]acetamide

InChI: InChI=1S/C12H15N3O6/c1-6(17)13-7-2-3-15(11(19)14-7)10-8-9(18)12(4-16,21-10)5-20-8/h2-3,8-10,16,18H,4-5H2,1H3,(H,13,14,17,19)/t8-,9+,10-,12+/m1/s1

Synonyms: N4-acetyl-2'-O-4'-C-Locked-cytidine; Acetamide, N-[1-[2,5-anhydro-4-C-(hydroxymethyl)-α-L-lyxofuranosyl]-1,2-dihydro-2-oxo-4-pyrimidinyl]-; LNA C(Ac)

N4-Dibutylformamidine-2'-O-Me-Cr

Description: N4-Dibutylformamidine-2'-O-Me-Cr is a modified nucleoside used in oligonucleotide synthesis. It consists of a dibutylformamidine group attached to the N4 position of cytosine, a methyl (Me) group at the 2' position of ribose, and a modified cytosine (Cr). This modification alters the properties of the oligonucleotide and can be utilized for specific applications in nucleic acid research and biotechnology.

CAT: BRP-00987

Molecular Formula: C19H32N4O5

Molecular Weight: 396.49

Purity: ≥98% by HPLC

Appearance: White powder

Size	Price	Stock	Quantity
--	--	--

Inquiry

Storage: Store at 2-8 °C, Keep in a dark and dry place

InChIKey: MMQXUCDIZCUQOH-VDHUWJSZSA-N

IUPAC Name: N,N-dibutyl-N'-(1-((2R,3R,4R,5R)-4-hydroxy-5-(hydroxymethyl)-3-methoxytetrahydrofuran-2-yl)-2-oxo-1,2-dihydropyrimidin-4-yl)formimidamide

InChI: InChI=1S/C19H32N4O5/c1-4-6-9-22(10-7-5-2)13-20-15-8-11-23(19(26)21-15)18-17(27-3)16(25)14(12-24)28-18/h8,11,13-14,16-18,24-25H,4-7,9-10,12H2,1-3H3/t14-,16-,17-,18-/m1/s1

Synonyms: N4-dibutylformamidine-2'-O-methyl-cytidine

2'-O-(2-Methoxyethyl)-5-methylcytidine hydrochloride

5'-O-DMT-5-Hydroxyethyl-dU

5'-O-DMT-2'-O-TBDMS-N2-ibu-L-rG

N6-Benzoyl-2',3'-di-O-acetyladenosine

(E)-N'-(1-Benzyl-9-((2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-6-oxo-6,9-dihydro-1H-purin-2-yl)-N,N-dimethylformimidamide

5,8-Dihydro-N,N,5-trimethyl-8-β-D-ribofuranosylpyrrolo[2',3':4,5]pyrrolo[2,3-d]pyrimidin-4-amine

5-O-DMT-N2-Dimethylformamide-2-O-methylguanosine

(E)-N2-Dimethylformamide-2-O-methylguanosine

[N(E)]-N-[(Dimethylamino)methylene]guanosine

2'-O-TBDMS-N2-DMF-rG

5-Bromotubercidin

O2',O3',O5'-Tribenzoyl-5-methyl-2-thiouridine

2',3'-O-Isopropylidenecytidine sulfate

1-(β-D-lyxofuranosyl)uracil

(E)-Ethyl 3-(1-((2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-5-yl)acrylate

6-Fluoro-3,4-dihydro-3-oxo-4-(2,3,5-tri-O-acetyl-β-D-ribofuranosyl)pyrazinecarboxamide

2-O-Ethyl-2'-O-methyluridine

S-(5')-Adenosyl-3-thiopropylamine

N4-Ac-2'-O-4'-C-Locked-Cr

N4-Dibutylformamidine-2'-O-Me-Cr

Our Products

Liposome Products

MicroRNA Products

mRNA Products

siRNA Products

RNA Synthesis Reagents

Cap Analogs

CPGs for Oligo Synthesis

Nucleosides

Nucleotides

Phosphoramidites