1289100-95-3

Basic information

• Product Name: phenyl 3,5-di-O-benzoyl-2-O-(chloroacetyl)-1-thio-α-D-arabinofuranoside
• Synonyms: phenyl 3,5-di-O-benzoyl-2-O-(chloroacetyl)-1-thio-α-D-arabinofuranoside
• CAS NO: 1289100-95-3
• Molecular Weight: 526.994
• Mol File: 1289100-95-3.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: phenyl 3,5-di-O-benzoyl-2-O-(chloroacetyl)-1-thio-α-D-arabinofuranoside(CAS DataBase Reference)
• NIST Chemistry Reference: phenyl 3,5-di-O-benzoyl-2-O-(chloroacetyl)-1-thio-α-D-arabinofuranoside(1289100-95-3)
• EPA Substance Registry System: phenyl 3,5-di-O-benzoyl-2-O-(chloroacetyl)-1-thio-α-D-arabinofuranoside(1289100-95-3)

Safety Data

• Hazardous Substances Data: 1289100-95-3(Hazardous Substances Data)

Upstream product

• 1379681-43-2 phenyl 3,5-di-O-benzoyl-1-thio-α-D-arabinofuranoside 
• 541-88-8 Chloroacetic anhydride 
• 1379681-42-1 phenyl 2-O-acetyl-3,5-di-O-benzoyl-1-thio-α-D-arabinofuranoside 
• 76612-55-0 1,2-di-O-acetyl-3,5-di-O-benzoyl-D-arabinofuranose 
• 1312541-22-2 3,5-di-O-benzoyl-1,2-O-benzylidene-β-D-arabinofuranose 
• 4348-68-9 2,3,5-tri-O-benzoyl-α-D-arabinofuranosyl bromide 
• 7473-42-9 methyl tri-O-benzoyl-α-D-arabinofuranoside 
• 1312541-23-3 3,5-di-O-benzoyl-1,2-bis-O-(chloroacetyl)-D-arabinofuranose 
• 108-98-5 thiophenol 
• 1379681-38-5 3,5-di-O-benzoyl-1,2-O-benzylidene-β-D-arabinofuranoside 

Downstream Products

• 1289100-92-0 C₇₅H₆₇Cl₃O₂₆ 

Relevant articles and documents

A practical silicon-free strategy for differentiation of hydroxy groups in arabinofuranose derivatives

Effective differentiation of 3,5-diol system and 2-hydroxy group in arabinofuranose derivatives, which is required for the preparation of building blocks useful for the synthesis of nucleoside analogues and oligosaccharide fragments of mycobacterial arabinogalactan and lipoarabinomannan, was achieved by using 3,5-di-O-benzoyl-1,2-O-benzylidene-βD-arabinofuranose or 3-O-(chloroacetyl)-β- d-arabinofuranose 1,2,5-orthobenzoate, both readily accessible from inexpensive methylα-d-arabinofuranoside via the corresponding glycosyl bromides. The use of expensive organosilicon protecting groups is completely avoided in this novel strategy, a feature that makes it amenable to scale-up. Georg Thieme Verlag Stuttgart New York.