540474-09-7

Basic information

• Product Name: allyl 2-O-benzoyl-4,6-O-benzylidene-β-D-glucopyranoside
• Synonyms: allyl 2-O-benzoyl-4,6-O-benzylidene-β-D-glucopyranoside
• CAS NO: 540474-09-7
• Molecular Weight: 412.439
• Mol File: 540474-09-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: allyl 2-O-benzoyl-4,6-O-benzylidene-β-D-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: allyl 2-O-benzoyl-4,6-O-benzylidene-β-D-glucopyranoside(540474-09-7)
• EPA Substance Registry System: allyl 2-O-benzoyl-4,6-O-benzylidene-β-D-glucopyranoside(540474-09-7)

Safety Data

• Hazardous Substances Data: 540474-09-7(Hazardous Substances Data)

Upstream product

• 98-88-4 benzoyl chloride 
• 20746-64-9 allyl (R)-4,6-O-benzylidene-β-D-gluco-pyranoside 

Downstream Products

• 1351219-29-8 allyl 2-O-benzoyl-4,6-O-benzylidene-3-O-levulinoyl-β-D-glucopyranosyl-(1->3)-2-O-benzoyl-4,6-O-benzylidene-β-D-glucopyranoside 
• 824402-82-6 allyl 3-O-acetyl-2-O-benzoyl-4,6-O-benzylidene-β-D-glucopyranosyl-(1->3)-2-O-benzoyl-4,6-O-benzylidene-β-D-glucopyranosyl-(1->3)-2-O-benzoyl-4,6-O-benzylidene-β-D-glucopyranoside 
• 824402-83-7 allyl 2-O-benzoyl-4,6-O-benzylidene-β-D-glucopyranosyl-(1->3)-2-O-benzoyl-4,6-O-benzylidene-β-D-glucopyranosyl-(1->3)-2-O-benzoyl-4,6-O-benzylidene-β-D-glucopyranoside 
• 824402-81-5 allyl 2-O-benzoyl-4,6-O-benzylidene-β-D-glucopyranosyl-(1->3)-2-O-benzoyl-4,6-O-benzylidene-β-D-glucopyranoside 
• 824402-80-4 allyl 3-O-acetyl-2-O-benzoyl-4,6-O-benzylidene-β-D-glucopyranosyl-(1->3)-2-O-benzoyl-4,6-O-benzylidene-β-D-glucopyranoside 

Relevant articles and documents

Synthesis of (R)-2,3-epoxypropyl(1→3)-β-D-pentaglucoside

The title pentasaccharide was synthesized via a 2 + 3 strategy. The disaccharide donor, 3-O-acetyl-2-O-benzoyl-4,6-O-benzylidene-β-d- glucopyranosyl-(1→3)-2-O-benzoyl-4,6-O-benzylidene-α-d- glucopyranosyl trichloroacetimidate (8), was obtained by selectiv

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