58781-27-4

Basic information

• Product Name: 2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl 2,3,4,6-tetra-O-benzyl-β-D-glucopyranoside
• Synonyms: 2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl 2,3,4,6-tetra-O-benzyl-β-D-glucopyranoside
• CAS NO: 58781-27-4
• Molecular Weight: 1063.3
• Mol File: 58781-27-4.mol
• Article Data: 19

Chemical Properties

• CAS DataBase Reference: 2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl 2,3,4,6-tetra-O-benzyl-β-D-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl 2,3,4,6-tetra-O-benzyl-β-D-glucopyranoside(58781-27-4)
• EPA Substance Registry System: 2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl 2,3,4,6-tetra-O-benzyl-β-D-glucopyranoside(58781-27-4)

Safety Data

• Hazardous Substances Data: 58781-27-4(Hazardous Substances Data)

Upstream product

• 53270-14-7 benzyl 2,3-O-isopropylidene-α-L-rhamnopyranoside 
• 4132-28-9 2,3,4,6-tetra-O-benzyl-D-mannopyranose 
• 4291-69-4 2,3,4,6-Tetra-O-benzyl-D-glucopyranose 
• 16475-29-9 phenylchlorosulfate 
• 139608-10-9 methyl 2,3,6-tri-O-benzyl-4-O-isopropenyl-α-D-glucopyranoside 
• 108-93-0 cyclohexanol 
• 82231-37-6 methyl 4-O-acetyl-2,3,6-tri-O-benzyl-α-D-glucopyranoside 
• 6207-45-0 2-allyloxy-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran 
• 872123-62-1 2,4-dinitro-6-(methoxycarbonyl)phenyl 2,3,4,6-tetra-O-benzyl-α,β-D-glucopyranoside 
• 6564-72-3 2,3,4,6-tetra-O-benzyl-D-glucopyranose 
• 139684-64-3 (Z)-prop-1'-enyl 2,3,4,6-tetra-O-benzyl-α-D-glucopyranoside 
• 89825-08-1 2,3,4,6-tetra-O-benzyl-1-O-trimethylsilyl-α,β-D-glucopyranose 
• 80-97-7 Cholestanol 
• 19488-48-3 methyl O-2,3,6-tri-O-benzyl-α-D-glucopyranoside 

Downstream Products

• 585-91-1 neotrehalose 

Relevant articles and documents

A dehydrative glycosylation protocol mediated by nonafluorobutanesulfonyl fluoride (NfF)

A new dehydrative glycosylation protocol that proceeds through selective activation of glycosyl hemiacetals with nonafluorobutanesulfonyl fluoride (NfF) has been disclosed. Contrary to the major classical glycosylation reactions that proceed under acidic

2-Allylphenyl glycosides as glycosyl donors for sugar coupling

Glycosylations employing 2-allylphenyl glycoside, a new type of stable glycosyl donor, were optimized and explored with a variety of acceptors promoted by ICl/AgOTf. The utility of the protocol was further demonstrated with an efficient synthesis of the disaccharide fragment of bleomycins.

2-Allyloxyphenyl glycoside as a new and stable type of glycosyl donors

A high-yielding coupling of a new and stable type of glycosyl donors, namely 2-allyloxyphenyl glycoside, with a variety of alcohols via NIS/TfOH reagent combination as effective activators at room temperature is described here.