127514-28-7

Basic information

• Product Name: Allyl 2-O-benzoyl-4,6-O-benzylidene-α-D-glucopyranoside
• Synonyms: Allyl 2-O-benzoyl-4,6-O-benzylidene-α-D-glucopyranoside
• CAS NO: 127514-28-7
• Molecular Weight: 412.439
• Mol File: 127514-28-7.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: Allyl 2-O-benzoyl-4,6-O-benzylidene-α-D-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: Allyl 2-O-benzoyl-4,6-O-benzylidene-α-D-glucopyranoside(127514-28-7)
• EPA Substance Registry System: Allyl 2-O-benzoyl-4,6-O-benzylidene-α-D-glucopyranoside(127514-28-7)

Safety Data

• Hazardous Substances Data: 127514-28-7(Hazardous Substances Data)

Upstream product

• 7464-56-4 1-O-allyl-α-D-glucopyranoside 
• 2280-44-6 D-Glucose 
• 98-88-4 benzoyl chloride 
• 93382-48-0 allyl 4,6-O-benzylidene-α-D-glucopyranoside 
• 93-97-0 benzoic acid anhydride 
• 263550-35-2 allyl 3-O-chloroacetyl-2-O-benzoyl-4,6-O-benzylidene-α-D-glucopyranoside 

Downstream Products

• 161423-95-6 allyl 2-O-benzoyl-3-O-(2,3,4-tri-O-benzoyl-α-L-rhamnopyranosyl)-4,6-O-benzylidene-α-D-glucopyranoside 
• 263550-35-2 allyl 3-O-chloroacetyl-2-O-benzoyl-4,6-O-benzylidene-α-D-glucopyranoside 
• 311349-77-6 allyl 4,6-di-O-acetyl-3-O-chloroacetyl-2-O-benzoyl-β-D-glucopyranosyl-(1->3)-2-O-benzoyl-4,6-O-benzylidene-α-D-glucopyranoside 
• 1351219-19-6 allyl 2-O-benzoyl-3-O-levulinoyl-α-D-glucopyranoside 
• 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 
• 1351219-37-8 allyl 2-O-acetyl-3,4,6-tri-O-benzyl-β-D-glucopyranosyl-(1->6)-4-O-acetyl-2-O-benzoyl-3-O-levulinoyl-α-D-glucopyranoside 
• 1351219-20-9 allyl 2-O-acetyl-3,4,6-tri-O-benzyl-β-D-glucopyranosyl-(1->6)-2-O-benzoyl-3-O-levulinoyl-α-D-glucopyranoside 
• 1351219-36-7 allyl 2-O-benzoyl-4,6-O-benzylidene-3-O-levulinoyl-α-D-glucopyranoside 
• 161423-96-7 allyl 2-O-benzoyl-3-O-(2,3,4-tri-O-benzoyl-α-L-rhamnopyranosyl)-α-D-glucopyranoside 
• 311349-80-1 C₅₉H₆₁ClO₂₄ 
• 311349-81-2 4,6-Di-O-acetyl-2-O-benzoyl-β-D-glucopyranosyl-(1->3)-2-O-benzoyl-4,6-O-benzylidene-β-D-gluco-pyranosyl-(1->3)-4,6-di-O-acetyl-2-O-benzoyl-α-D-glucopyranoside 

Relevant articles and documents

Assembly of a β-(1?→?3)-glucan laminarihexaose on ionic liquid support

An efficient method for the preparation of β-(1?→?3)-D-glucan laminarihexaose on ionic liquid (IL)-support is described. A β-(1?→?3)-glucan laminarihexaose was rapidly assembled in 15?h in a stereoselective fashion with an average yield of over 90% per st

Synthesis, (1→3)-β-d-glucanase-binding ability and phytoalexin-elicitor activity of (R)-2,3-epoxypropyl (1→3)-β-d- pentaglucoside

The (1→3)-β-d-pentaglucoside was synthesized as its (R)-2,3-epoxypropyl glycoside via 2 + 3 strategy. The disaccharide donor 8 was obtained by 3-selective coupling of 2 with 4, followed by deallylation, and trichloroacetimidation. Meanwhile, the trisaccha

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