155786-67-7

Basic information

• Product Name: 1,3,4,6-tetra-O-acetyl-2-O-(2,3,4-tri-O-benzoyl-α-D-glucopyranosyl)-α-D-glucopyranose
• Synonyms: 1,3,4,6-tetra-O-acetyl-2-O-(2,3,4-tri-O-benzoyl-α-D-glucopyranosyl)-α-D-glucopyranose
• CAS NO: 155786-67-7
• Molecular Weight: 822.774
• Mol File: 155786-67-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1,3,4,6-tetra-O-acetyl-2-O-(2,3,4-tri-O-benzoyl-α-D-glucopyranosyl)-α-D-glucopyranose(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3,4,6-tetra-O-acetyl-2-O-(2,3,4-tri-O-benzoyl-α-D-glucopyranosyl)-α-D-glucopyranose(155786-67-7)
• EPA Substance Registry System: 1,3,4,6-tetra-O-acetyl-2-O-(2,3,4-tri-O-benzoyl-α-D-glucopyranosyl)-α-D-glucopyranose(155786-67-7)

Safety Data

• Hazardous Substances Data: 155786-67-7(Hazardous Substances Data)

Upstream product

• 4196-35-4 2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl bromide 
• 118646-78-9 Acetic acid (2R,3R,4S,5R,6R)-2,5-diacetoxy-6-acetoxymethyl-3-((2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-4-yl ester 
• 100644-74-4 1,3,4,6-tetra-O-acetyl-2-O-(2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl)-α-D-glucopyranose 
• 54423-54-0 2,3,4,6-Tetra-O-benzyl 1-O-p-nitrobenzoyl D-glucopyranoside 
• 155786-66-6 1,3,4,6-tetra-O-acetyl-2-O-(2,3,4-tri-O-benzoyl-6-O-trityl-α-D-glucopyranosyl)-α-D-glucopyranose 

Downstream Products

• 155786-69-9 3,4,6-tri-O-acetyl-2-O-(2,3,4-tri-O-benzoyl-6-O-chloroacetyl-α-D-glucopyranosyl)-α-D-glucopyranosyl bromide 
• 155786-72-4 3,4,6-tri-O-acetyl-2-O-(2,3,4-tri-O-benzoyl-6-O-chloroacetyl-α-D-glucopyranosyl)-β-D-glucopyranosyl trichloroacetamidate 
• 155786-73-5 allyl O-(2,3,4-tri-O-benzoyl-α-D-glucopyranosyl)-(1<*>2)-O-(3,4,6-tri-O-acetyl-α-D-glucopyranosyl)-(1<*>3)-2-O-benzoyl-4,6-benzylidene-α-D-glucopyranoside 
• 155786-68-8 1,3,4,6-tetra-O-acetyl-2-O-(2,3,4-tri-O-benzoyl-6-O-chloroacetyl-α-D-glucopyranosyl)-α-D-glucopyranose 

Relevant articles and documents

Synthesis of linear oligosaccharides: L-glycero-α-D-manno-heptopyranosyl derivatives of allyl α-glycosides of D-glucose, kojibiose, and 3-O-α-kojibiosyl-D-glucose, substrates for synthetic antigens

Synthesis of the title oligosaccharides was performed with the use of peracetylated L-glycero-β-D-manno-heptosyl trichloroacetamidate as the heptosyl donor and (oligo)glucosyl acceptors bearing acyl and acetal protecting groups.