161110-15-2

Basic information

• Product Name: N⁴-2-(4-nitrophenyl)ethoxycarbonyl-3'-deoxycytidi
• CAS NO: 161110-15-2
• Molecular Weight: 420.379
• Mol File: 161110-15-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N⁴-2-(4-nitrophenyl)ethoxycarbonyl-3'-deoxycytidi(CAS DataBase Reference)
• NIST Chemistry Reference: N⁴-2-(4-nitrophenyl)ethoxycarbonyl-3'-deoxycytidi(161110-15-2)
• EPA Substance Registry System: N⁴-2-(4-nitrophenyl)ethoxycarbonyl-3'-deoxycytidi(161110-15-2)

Safety Data

• Hazardous Substances Data: 161110-15-2(Hazardous Substances Data)

Upstream product

• 88091-70-7 1-methyl-3-[2-(4-nitrophenyl)ethoxycarbonyl]imidazolium chloride 
• 7057-33-2 3'-deoxycytidine 
• 54925-66-5 2',5'-bis-O-(tert-butyldimethylsilyl)uridine 
• 19312-45-9 2',5'-di-O-acetyl-3'-deoxyuridine 
• 58-96-8 uridine 
• 161109-93-9 3'-O-phenoxythiocarbonyl-2'-O-thexyldimethylsilyl-5'-O-trityluridine 
• 161109-82-6 2'-O-thexyldimethylsilyl-5'-O-trityluridine 
• 161110-03-8 3'-O-phenoxythiocarbonyl-2',5'-di-O-thexyldimethylsilyluridine 
• 161110-04-9 1-[2,5-O-bis(tert-butyldimethylsilyl)-3-O-phenylthiocarbonyl-β-D-pentofuranosyl]-uracyl 
• 161109-90-6 1-{(2R,3R,4R,5R)-3-[Dimethyl-(1,1,2-trimethyl-propyl)-silanyloxy]-5-[dimethyl-(1,1,2-trimethyl-propyl)-silanyloxymethyl]-4-hydroxy-tetrahydro-furan-2-yl}-1H-pyrimidine-2,4-dione 
• 161109-94-0 N⁴,2'-di-N,O-acetyl-3'-deoxy-5'-O-(4-methylbenzoyl)-cytidine 
• 161109-95-1 1-(2,5-di-O-acetyl-3-deoxy-β-D-erythro-pentofuranosyl)-4-(1,2,4-triazol-1-yl)-2(1H)-pyrimidone 
• 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 
• 161110-11-8 2',5'-di-O-acetyl-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.