144950-26-5

Basic information

• Product Name: 2,3,5-tri-O-benzyl-L-lyxose dibenzyldithioacetal
• Synonyms: 2,3,5-tri-O-benzyl-L-lyxose dibenzyldithioacetal
• CAS NO: 144950-26-5
• Molecular Weight: 650.903
• Mol File: 144950-26-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2,3,5-tri-O-benzyl-L-lyxose dibenzyldithioacetal(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3,5-tri-O-benzyl-L-lyxose dibenzyldithioacetal(144950-26-5)
• EPA Substance Registry System: 2,3,5-tri-O-benzyl-L-lyxose dibenzyldithioacetal(144950-26-5)

Safety Data

• Hazardous Substances Data: 144950-26-5(Hazardous Substances Data)

Upstream product

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

Downstream Products

• 158852-11-0 benzyl 2,3,5-tri-O-benzyl-1,4-dithio-D-ribofuranoside 
• 161424-52-8 9-(2,3,5-tri-O-benzyl-4-thio-α-D-ribofuranosyl)-adenine 
• 161424-53-9 9-(2,3,5-tri-O-benzyl-4-thio-β-D-ribofuranosyl)-adenine 
• 161424-54-0 1-(4-thio-α-D-ribofuranosyl)-N₄-benzoyl-cytosine 
• 159981-07-4 N⁴-benzoyl-1-(4-thio-β-D-ribo-pentofuranosyl)cytosine 
• 4303-00-8 1-(4-thio-α-D-ribofuranosyl)-adenine 
• 2500-80-3 (2R,3R,4S,5R)-2-(6-amino-9H-purin-9-yl)-5-(hydroxymethyl)tetrahydrothiophene-3,4-diol 
• 93080-09-2 4'-thiocytidine 
• 144950-27-6 Methanesulfonic acid (1S,2S,3R)-2,3-bis-benzyloxy-1-benzyloxymethyl-4,4-bis-benzylsulfanyl-butyl ester 

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.

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