95906-49-3

Basic information

• Product Name: 5'-O-trityl-3'-deoxyuridine
• Synonyms: 5'-O-trityl-3'-deoxyuridine
• CAS NO: 95906-49-3
• Molecular Weight: 470.525
• Mol File: 95906-49-3.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 5'-O-trityl-3'-deoxyuridine(CAS DataBase Reference)
• NIST Chemistry Reference: 5'-O-trityl-3'-deoxyuridine(95906-49-3)
• EPA Substance Registry System: 5'-O-trityl-3'-deoxyuridine(95906-49-3)

Safety Data

• Hazardous Substances Data: 95906-49-3(Hazardous Substances Data)

Upstream product

• 58-96-8 uridine 
• 76-83-5 trityl chloride 
• 130860-11-6 2'-O-(tert-butyldimethylsilyl)-3'-O-(phenoxythiocarbonyl)-5'-O-trityluridine 
• 117136-35-3 2'-O-(tert-butyldimethylsilyl)-5'-O-(triphenylmethyl)uridine 
• 130860-12-7 2'-O-(tert-butyldimethylsilyl)-3'-deoxy-5'-O-trityluridine 
• 6554-10-5 5'-O-trityluridine 
• 130860-04-7 2,2'-anhydro-1-<3-O-(phenoxythiocarbonyl)-5-O-trityl-β-D-threo-pentofuranosyl>uracil 
• 3249-94-3 5′-O-trityl-2,2′-anhydro-β-D-uridine 
• 130860-05-8 2,2'-anhydro-1-(3-deoxy-5-O-trityl-β-D-threo-pentofuranosyl)uracil 
• 161109-93-9 3'-O-phenoxythiocarbonyl-2'-O-thexyldimethylsilyl-5'-O-trityluridine 
• 161109-82-6 2'-O-thexyldimethylsilyl-5'-O-trityluridine 

Downstream Products

• 95906-48-2 1-(5'-O-triphenylmethyl-3'-deoxy-β-D-glycero-pentofuran-2-ulosyl)uracil 
• 86234-45-9 N⁴-benzoyl-5'-O-dimethoxytrityl-3'-deoxyribicytidine 
• 7057-33-2 3'-deoxycytidine 
• 161110-00-5 N⁴-benzoyl-3'-deoxyribicytidine 
• 161110-15-2 N⁴-2-(4-nitrophenyl)ethoxycarbonyl-3'-deoxycytidi 
• 7057-27-4 3'-deoxyuridine 
• 130860-06-9 1-(2-O-acetyl-3-deoxy-5-O-trityl-β-D-threo-pentofuranosyl)uracil 

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.