106568-79-0

Basic information

• Product Name: 3'-5'-DI-O-ACETYL-2'-DEOXYINOSINE
• Synonyms: 3'-5'-DI-O-ACETYL-2'-DEOXYINOSINE
• CAS NO: 106568-79-0
• Molecular Formula: C₁₄H₁₆N₄O₆
• Molecular Weight: 336.3
• Mol File: 106568-79-0.mol
• Article Data: 7

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 3'-5'-DI-O-ACETYL-2'-DEOXYINOSINE(CAS DataBase Reference)
• NIST Chemistry Reference: 3'-5'-DI-O-ACETYL-2'-DEOXYINOSINE(106568-79-0)
• EPA Substance Registry System: 3'-5'-DI-O-ACETYL-2'-DEOXYINOSINE(106568-79-0)

Safety Data

• Hazardous Substances Data: 106568-79-0(Hazardous Substances Data)

Upstream product

• 890-38-0 2-deoxyinosine 
• 108-24-7 acetic anhydride 
• 112-55-0 1-dodecylthiol 
• 17318-24-0 3',5'-di-O-acetyl-2'-deoxyadenosine 
• 958-09-8 2'-deoxy-D-adenosine 

Downstream Products

• 342630-71-1 5'-O-(4,4'-Dimethoxytrityl)-N⁶-(1-oxyl-2,2,6,6-tetramethyl-4-piperidinyl)-2'-deoxyadenosine 
• 145060-61-3 5'-O-(4,4'-dimethoxytriphenylmethyl)-2'-deoxy-6-(2,4-dinitrophenyl)thiopurine-3'-O-(2-cyanoethyl-N,N-diisopropylamino)-phosphoramidite 
• 145060-62-4 (2R,3S,5R)-2-[Bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-5-[6-(2,4-dinitro-phenylsulfanyl)-purin-9-yl]-tetrahydro-furan-3-ol 
• 145060-60-2 (2R,3S,5R)-5-[6-(2,4-Dinitro-phenylsulfanyl)-purin-9-yl]-2-hydroxymethyl-tetrahydro-furan-3-ol 
• 2239-64-7 6-mercaptopurine-2’-deoxyribose 
• 143417-17-8 C₅₆H₆₆N₇O₇PSi 
• 143417-16-7 C₄₇H₄₉N₅O₆Si 
• 143417-14-5 3',5'-di-O-acetyl-N⁶-tert-butyldiphenylsilyloxy-2'-deoxyadenosine 
• 143417-15-6 2'-deoxy-N⁶-tert-butyldiphenylsilyloxyadenosine 
• 114988-06-6 N⁶-(carbamoylmethyl)-2'-deoxy-5'-O-(4,4'-dimethoxytriphenylmethyl)adenosine 
• 89014-18-6 (-)-N⁶-(carbamoylmethyl)-2'-deoxyadenosine 
• 958-09-8 2'-deoxy-D-adenosine 
• 87202-41-3 6-amino-1-(2'-deoxy-β-D-erythro-pentofuranosyl)-1H-imidazo<4,5-c>pyridin-4(5H)-one 
• 78582-17-9 4-Amino-1-(2-deoxy-β-D-erythropentofuranosyl)-1H-imidazo<4,5-c>pyridine 

Relevant articles and documents

Preparation of oligodeoxynucleotides containing 6-methylthiopurine residues by chemical synthesis or specific methylation

Two methods (chemical synthesis and specific methylation) are described for the preparation of oligodeoxynucleotides containing 6-methylthiopurine residues. 6-Methylthiopurine phosphoramidite (6) is prepared and incorporated into oligomers. Methylation with methyl iodide of 6-thiopurine (or 6-thioguanine) in oligonucleotides also leads to exclusive production of 6-methylthiopurine (or 6-methylthioguanine) oligomers.

Nucleophile-catalyzed additions to activated triple bonds. protection of lactams, imides, and nucleosides with MocVinyl and related groups

Additions of lactams, imides, (S)-4-benzyl-1,3-oxazolidin-2-one, 2-pyridone, pyrimidine-2,4-diones (AZT derivatives), or inosines to the electron-deficient triple bonds of methyl propynoate, tert-butyl propynoate, 3-butyn-2-one, N-propynoylmorpholine, or

An efficient method for the synthesis of [4-15N]cytidine, 2'-deoxy[4-15N]cytidine, [6-15N]adenosine, and 2'-deoxy[6-15N]adenosine derivatives

Nucleophilic substitution reactions of 4-azolyl-1-β-D-ribofuranosylpyrimidin-2(1H)-one and 6-azolyl-9-β-D-ribofuranosyl-9H-purine derivatives, which were converted from uridine and inosine, with [15N]phthalimide in the presence of triethylamine