864967-07-7

Basic information

• Product Name: methyl 2,3,4-tri-O-benzyl-6-O-(4,6-di-O-benzyl-2,3-O-carbonyl-β-D-glucopyranosyl)-(1->6)-α-D-glucopyranoside
• CAS NO: 864967-07-7
• Molecular Weight: 832.945
• Mol File: 864967-07-7.mol

Chemical Properties

• CAS DataBase Reference: methyl 2,3,4-tri-O-benzyl-6-O-(4,6-di-O-benzyl-2,3-O-carbonyl-β-D-glucopyranosyl)-(1->6)-α-D-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 2,3,4-tri-O-benzyl-6-O-(4,6-di-O-benzyl-2,3-O-carbonyl-β-D-glucopyranosyl)-(1->6)-α-D-glucopyranoside(864967-07-7)
• EPA Substance Registry System: methyl 2,3,4-tri-O-benzyl-6-O-(4,6-di-O-benzyl-2,3-O-carbonyl-β-D-glucopyranosyl)-(1->6)-α-D-glucopyranoside(864967-07-7)

Safety Data

• Hazardous Substances Data: 864967-07-7(Hazardous Substances Data)

Upstream product

• 864966-87-0 phenyl 4,6-di-O-benzyl-2,3-O-carbonyl-1-thio-β-D-glucopyranoside 
• 53008-65-4 methyl 2,3,4-tri-O-benzyl-D-glucopyranoside 
• 1380233-75-9 p-tolyl 4,6-di-O-benzyl-1-thio-β-D-glucopyranoside 
• 1380233-76-0 p-tolyl 4,6-di-O-benzyl-2,3-O-carbonyl-1-thio-β-D-glucopyranoside 
• 1380233-69-1 p-tolyl 2,3-di-O-(4-methoxybenzyl)-1-thio-β-D-glucopyranoside 
• 1380233-68-0 p-tolyl 4,6-O-benzylidene-2,3-di-O-(4-methoxybenzyl)-1-thio-β-D-glucopyranoside 
• 1380233-74-8 p-tolyl 4,6-di-O-benzyl-2,3-di-O-p-methoxybenzyl-1-thio-β-Dglucopyranoside 
• 2936-70-1 (2R,3S,4S,5R,6S)-2-Hydroxymethyl-6-phenylsulfanyl-tetrahydro-pyran-3,4,5-triol 
• 864966-92-7 phenyl 4,6-di-O-benzyl-1-thio-β-D-glucopyranoside 
• 864966-90-5 phenyl 2,3-di-O-(2,3-dimethoxybutane-2,3-diyl)-1-thio-β-D-glucopyranoside 
• 864966-91-6 phenyl 4,6-di-O-benzyl-2,3-O-(2′,3′-dimethoxybutane-2′,3′-diyl)-1-thio-β-D-glucopyranoside 

Relevant articles and documents

Lewis acids as α-directing additives in glycosylations by using 2,3-O-carbonate-protected glucose and galactose thioglycoside donors based on preactivation protocol

Catalytic or stoichiometric amounts of Lewis acids were found to be very effective α-directing additives in the stereoselective glycosylations of diverse 2,3-O-carbonate-protected glucose and galactose thioglycoside donors by preactivation protocol. The p

Stereocontrolled formation of β-glucosides and related linkages in the absence of neighboring group participation: Influence of a trans-fused 2,3-O-carbonate group

Phenyl 4,6-di-O-benzyl-2,3-O-carbonyl-β-D-glucothiopyranoside and the regiosiomeric phenyl 2,6-di-O-benzyl-3,4-O-carbonyl-β-D-glucothiopyranoside were prepared and studied as glucosyl donors at -60 °C in dichloromethane with preactivation by 1-benzenesulf