161109-94-0

Basic information

• Product Name: N⁴,2'-di-N,O-acetyl-3'-deoxy-5'-O-(4-methylbenzoyl)-cytidine
• CAS NO: 161109-94-0
• Molecular Weight: 429.43
• Mol File: 161109-94-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N⁴,2'-di-N,O-acetyl-3'-deoxy-5'-O-(4-methylbenzoyl)-cytidine(CAS DataBase Reference)
• NIST Chemistry Reference: N⁴,2'-di-N,O-acetyl-3'-deoxy-5'-O-(4-methylbenzoyl)-cytidine(161109-94-0)
• EPA Substance Registry System: N⁴,2'-di-N,O-acetyl-3'-deoxy-5'-O-(4-methylbenzoyl)-cytidine(161109-94-0)

Safety Data

• Hazardous Substances Data: 161109-94-0(Hazardous Substances Data)

Upstream product

• 532-20-7 α-D-xylofuranose 
• 75096-60-5 1,2-O-isopropylidene-5-O-(4-toluoyl)-D-xylofuranose 
• 171603-61-5 4-Methyl-benzoic acid (3aR,5R,6S,6aR)-2,2-dimethyl-6-phenoxythiocarbonyloxy-tetrahydro-furo[2,3-d][1,3]dioxol-5-ylmethyl ester 
• 161110-10-7 3-deoxy-1,2-O-isopropylidene-5-O-(4-methylbenzoyl)-α-D-erythro-pentofuranose 
• 20031-21-4 1,2-O-isopropylidene-α-D-xylose 
• 14631-20-0 4-N-Acetylcytosine 
• 142823-65-2 1,2-di-O-acetyl-3-deoxy-5-O-(4-methylbenzoyl)-D-α,β-xylofuranose 

Downstream Products

• 86234-45-9 N⁴-benzoyl-5'-O-dimethoxytrityl-3'-deoxyribicytidine 
• 161110-00-5 N⁴-benzoyl-3'-deoxyribicytidine 
• 161110-15-2 N⁴-2-(4-nitrophenyl)ethoxycarbonyl-3'-deoxycytidi 
• 7057-33-2 3'-deoxycytidine 

Relevant articles and documents

Nucleosides. LVI. Synthesis and chemical modifications of 3'-deoxy- pyrimidine nucleosides

3'-Deoxyuridine(1) and 3'-deoxycytidine(2) were prepared with improved yields by two different methods applying either the Barton procedure to appropriate 2',5'-di-O-protected pyrimidine nucleosides or by choosing the direct glycosylation of the pyrimidine bases with 1,2-di-O-acetyl-5-O- toluoyl-3-deoxy-D-erythro-pentofuranose via the silylation approach. Suitable protecting groups for the sugar moiety have been found in the trityl, tert- butyldimethylsilyl and the thexyl groups which are inert in the radical deoxygenation process. The newly synthesised compounds were characterized by elemental analyses and UV and 1H-NMR spectra.