163180-51-6

Basic information

• Product Name: 3-O-benzoyl-4,6-benzylidene β-methyl-D-mannopyranoside
• Synonyms: 3-O-benzoyl-4,6-benzylidene β-methyl-D-mannopyranoside
• CAS NO: 163180-51-6
• Molecular Weight: 386.401
• Mol File: 163180-51-6.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 3-O-benzoyl-4,6-benzylidene β-methyl-D-mannopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: 3-O-benzoyl-4,6-benzylidene β-methyl-D-mannopyranoside(163180-51-6)
• EPA Substance Registry System: 3-O-benzoyl-4,6-benzylidene β-methyl-D-mannopyranoside(163180-51-6)

Safety Data

• Hazardous Substances Data: 163180-51-6(Hazardous Substances Data)

Upstream product

• 138811-32-2 methyl 3-O-benzoyl-4,6-O-benzylidene-β-D-glucopyranoside 
• 3162-96-7 Methyl-4,6-O-(phenylmethylene)-β-D-mannopyranoside 
• 98-88-4 benzoyl chloride 

Relevant articles and documents

Control of the ambident reactivity of the nitrite ion

In previous studies, it was reported that a neighbouring equatorial ester group is essential for a good yield of nitrite-mediated triflate inversion, whereas with neighbouring benzyl ether groups or axial ester groups, mixtures are generally produced. In

Regioselective benzoylation of 6-O-protected and 4,6-O-diprotected hexopyranosides as promoted by chiral and achiral ditertiary 1,2-diamines

Monobenzoylation of triols (6-O-silylated glycopyranosides) or diols (4,6-O-benzylidenated glycopyranosides) with benzoyl chloride and triethylamine at - 60° to 23° is promoted by catalytic amounts of ditertiary 1,2-diamines. The regioselectivity depends