666727-74-8

Basic information

• Product Name: 3-O-acetyl-2-O-benzoyl-4,6-O-benzylidene-α-D-glucopyranosyl trichloroacetimidate
• Synonyms: 3-O-acetyl-2-O-benzoyl-4,6-O-benzylidene-α-D-glucopyranosyl trichloroacetimidate
• CAS NO: 666727-74-8
• Molecular Weight: 558.8
• Mol File: 666727-74-8.mol

Chemical Properties

• CAS DataBase Reference: 3-O-acetyl-2-O-benzoyl-4,6-O-benzylidene-α-D-glucopyranosyl trichloroacetimidate(CAS DataBase Reference)
• NIST Chemistry Reference: 3-O-acetyl-2-O-benzoyl-4,6-O-benzylidene-α-D-glucopyranosyl trichloroacetimidate(666727-74-8)
• EPA Substance Registry System: 3-O-acetyl-2-O-benzoyl-4,6-O-benzylidene-α-D-glucopyranosyl trichloroacetimidate(666727-74-8)

Safety Data

• Hazardous Substances Data: 666727-74-8(Hazardous Substances Data)

Upstream product

• 127514-28-7 Allyl 2-O-benzoyl-4,6-O-benzylidene-α-D-glucopyranoside 
• 666727-73-7 allyl 3-O-acetyl-2-O-benzoyl-4,6-O-benzylidene-α-D-glucopyranoside 
• 98-88-4 benzoyl chloride 
• 93382-48-0 allyl 4,6-O-benzylidene-α-D-glucopyranoside 
• 545-06-2 trichloroacetonitrile 

Downstream Products

• 666727-75-9 allyl 3-O-acetyl-2-O-benzoyl-4,6-O-benzylidene-β-D-glucopyranosyl-(1->3)-2-O-benzoyl-4,6-O-benzylidene-α-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 
• 666727-80-6 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 
• 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

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