151662-55-4

Basic information

• Product Name: phenyl 2,3:4,6-bis-O-isopropylidene-1-thio-β-D-mannopyranoside
• Synonyms: phenyl 2,3:4,6-bis-O-isopropylidene-1-thio-β-D-mannopyranoside
• CAS NO: 151662-55-4
• Molecular Weight: 352.452
• Mol File: 151662-55-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: phenyl 2,3:4,6-bis-O-isopropylidene-1-thio-β-D-mannopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: phenyl 2,3:4,6-bis-O-isopropylidene-1-thio-β-D-mannopyranoside(151662-55-4)
• EPA Substance Registry System: phenyl 2,3:4,6-bis-O-isopropylidene-1-thio-β-D-mannopyranoside(151662-55-4)

Safety Data

• Hazardous Substances Data: 151662-55-4(Hazardous Substances Data)

Upstream product

• 68791-15-1 2,3:4,6-di-O-isopropylidene-α-D-mannopyranose 
• 77481-63-1 phenyl-1-thio-β-D-mannopyranoside 
• 77-76-9 2,2-dimethoxy-propane 
• 108-98-5 thiophenol 
• 132032-62-3 C₁₈H₃₇N₃O₆P⁽¹⁺⁾*Cl^(1-) 

Downstream Products

• 180699-36-9 C₁₈H₂₄O₆S 
• 405290-57-5 phenyl 4,6-di-O-acetyl-2-azido-3-O-benzoyl-2-deoxy-1-thio-β-D-glucopyranoside 
• 405290-56-4 phenyl 4,6-di-O-acetyl-3-O-benzoyl-1-thio-β-D-mannopyranoside 
• 246875-59-2 phenyl 4,6-di-O-acetyl-2,3-O-isopropylidne-1-thio-β-D-mannopyranoside 
• 246875-61-6 phenyl 4,6-di-O-acetyl-1-thio-β-D-mannopyranoside 
• 166516-67-2 phenyl 2-azido-2-deoxy-1-thio-β-D-glucopyranoside 
• 77481-63-1 phenyl-1-thio-β-D-mannopyranoside 

Relevant articles and documents

Synthesis of pyranoid and furanoid glycals from glycosyl sulfoxides by treatment with organolithium reagents

Glycosyl sulfoxides can be conveniently transformed into pyranoid or furanoid glycals by treatment with organolithium reagents. The more likely reaction pathway involves a sulfoxide/metal exchange reaction to generate a glycosyllithium derivative that und

Alkyloxytris(dimethylamino)phosphonium Salts. Part 21. Anomeric Hydroxy-group Activation of 2,3:4,6-Di-O-isopropylidene-α-D-mannopyranose, Thioglycosylation and Glycosylation

The action of carbon tetrachloride and tris(dimethylamino)phosphine at low temperature on 2,3:4,6-di-O-isopropylidene-α-D-mannopyranose affords the α anomeric form of the corresponding alkoxytris(dimethylamino)phosphonium chloride.The condensation of arom