158852-11-0

Basic information

• Product Name: benzyl 2,3,5-tri-O-benzyl-1,4-dithio-D-ribofuranoside
• Synonyms: benzyl 2,3,5-tri-O-benzyl-1,4-dithio-D-ribofuranoside
• CAS NO: 158852-11-0
• Molecular Weight: 542.763
• Mol File: 158852-11-0.mol

Chemical Properties

• CAS DataBase Reference: benzyl 2,3,5-tri-O-benzyl-1,4-dithio-D-ribofuranoside(CAS DataBase Reference)
• NIST Chemistry Reference: benzyl 2,3,5-tri-O-benzyl-1,4-dithio-D-ribofuranoside(158852-11-0)
• EPA Substance Registry System: benzyl 2,3,5-tri-O-benzyl-1,4-dithio-D-ribofuranoside(158852-11-0)

Safety Data

• Hazardous Substances Data: 158852-11-0(Hazardous Substances Data)

Upstream product

• 158814-04-1 Benzoic acid (1S,2R,3R)-2,3-bis-benzyloxy-1-benzyloxymethyl-4,4-bis-benzylsulfanyl-butyl ester 
• 100-53-8 phenylmethanethiol 
• 16838-89-4 2,3,5-tri-O-benzyl-D-ribofuranose 
• 161424-49-3 2,3,5-tri-O-benzyl-4-O-p-nitrobenzoyl-L-lyxose dithiobenzylacetal 
• 64363-77-5 methyl 2,3,5-tri-O-benzyl-D-ribofuranoside 
• 144950-26-5 2,3,5-tri-O-benzyl-L-lyxose dibenzyldithioacetal 
• 153439-75-9 2,3,5-tri-O-benzyl-D-ribose dibenzyldithioacetal 

Downstream Products

• 93080-09-2 4'-thiocytidine 
• 2500-80-3 (2R,3R,4S,5R)-2-(6-amino-9H-purin-9-yl)-5-(hydroxymethyl)tetrahydrothiophene-3,4-diol 
• 4303-00-8 1-(4-thio-α-D-ribofuranosyl)-adenine 
• 159981-07-4 N⁴-benzoyl-1-(4-thio-β-D-ribo-pentofuranosyl)cytosine 
• 161424-54-0 1-(4-thio-α-D-ribofuranosyl)-N₄-benzoyl-cytosine 
• 161424-53-9 9-(2,3,5-tri-O-benzyl-4-thio-β-D-ribofuranosyl)-adenine 
• 161424-52-8 9-(2,3,5-tri-O-benzyl-4-thio-α-D-ribofuranosyl)-adenine 
• 161424-50-6 1-<2,3,5-tri-O-benzyl-4-thio-α-D-ribofuranosyl>-N₄-benzoyl-cytosine 
• 161424-51-7 1-<2,3,5-tri-O-benzyl-4-thio-β-D-ribofuranosyl>-N₄-benzoyl-cytosine 
• 161512-40-9 1-O-acetyl-2,3,5-tri-O-benzyl-4-thio-α,β-D-ribofuranose 

Relevant articles and documents

The synthesis and biological activity of certain 4'-thionucleosides

Results are presented on the synthesis and biological activity of several types of 4'-thionucleosides as potential anticancer agents. Detailed studies on the mechanism of action of 4'-thiothymidine are also presented.

A new synthesis of some 4'-thio-D-ribonucleosides and preliminary enzymatic evaluation

A new synthesis of 4'-thioribonucleosides is presented together with the enzymatic evaluation of the adenosine analogues with respect to adenosine kinase. The 4-thio-D-ribofuranosyl carbohydrate precursor 7 was obtained in good yield from D-ribose and fur

Synthesis and biological activity of 4'-thionucleosides of 2- chloroadenine

1,2,3,5-Tetra-O-acetyl-4-thio-D-ribofuranose, prepared from 2,3,5-tri-O- benzyl-D-ribofuranose in four steps, was converted to the corresponding 2- chloroadenine nucleoside (8), which was deoxygenated to obtain 2-chloro-2'- deoxy-4'-thioadenosine (12). Th