115649-78-0

Basic information

• Product Name: 1,2-dideoxy-4,5,7-tri-O-benzyl-D-galacto-1-heptenitol
• Synonyms: 1,2-dideoxy-4,5,7-tri-O-benzyl-D-galacto-1-heptenitol
• CAS NO: 115649-78-0
• Molecular Weight: 448.559
• Mol File: 115649-78-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1,2-dideoxy-4,5,7-tri-O-benzyl-D-galacto-1-heptenitol(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-dideoxy-4,5,7-tri-O-benzyl-D-galacto-1-heptenitol(115649-78-0)
• EPA Substance Registry System: 1,2-dideoxy-4,5,7-tri-O-benzyl-D-galacto-1-heptenitol(115649-78-0)

Safety Data

• Hazardous Substances Data: 115649-78-0(Hazardous Substances Data)

Upstream product

• 20672-66-6 3,4,5-tri-O-benzyl-D-galactopyranose 
• 1779-49-3 Methyltriphenylphosphonium bromide 
• 1826-67-1 vinyl magnesium bromide 
• 16838-89-4 2,3,5-tri-O-benzyl-D-lyxofuranoside 

Downstream Products

• 1621703-79-4 (2α,3S,4R,5S,6R)-4,5-bis(benzyloxy)-6-((benzyloxy)methyl)-2-vinyltetrahydro-2H-pyran-3-ol 
• 77737-59-8 (2β,3S,4R,5S,6R)-4,5-bis(benzyloxy)-6-((benzyloxy)methyl)-2-vinyltetrahydro-2H-pyran-3-ol 
• 240415-65-0 (1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-acetic acid (3R,4S,5S,6R)-4,5-bis-benzyloxy-6-benzyloxymethyl-2-methylene-tetrahydro-pyran-3-yl ester 
• 240415-64-9 tert-Butoxycarbonylamino-acetic acid (3R,4S,5S,6R)-4,5-bis-benzyloxy-6-benzyloxymethyl-2-methylene-tetrahydro-pyran-3-yl ester 
• 240415-63-8 Propionic acid (3R,4S,5S,6R)-4,5-bis-benzyloxy-6-benzyloxymethyl-2-methylene-tetrahydro-pyran-3-yl ester 
• 240415-47-8 Acetic acid (3R,4S,5S,6R)-4,5-bis-benzyloxy-6-benzyloxymethyl-2-methylene-tetrahydro-pyran-3-yl ester 
• 240415-45-6 (3R,4R,5S,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-2-methylene-tetrahydro-pyran-3-ol 

Relevant articles and documents

Highly stereoselective synthesis of C-vinyl pyranosides via a Pd 0-mediated cycloetherification of 1-acetoxy-2,3-dideoxy-oct-2-enitols

Oct-2-enitols undergo a Pd0-mediated cyclization to produce C-vinyl α-gluco- and α-galactopyranosides, and C-vinyl β-mannopyranoside in good yield and with high stereoselectivity. While substrate control demonstrates a clear stereochemical pref

Vinylation-Electrophilic Cyclization of Aldopentoses: Easy and Stereoselective Access to C-Glycopyranosides of Rare Sugars

A new C-glycosylation procedure, which involves vinylation of a properly protected aldopentose and mercuriocyclization of the obtained glycoenitol, is described; it allows C-glycopyranosides of rare sugars to be obtained from easily available pentoses. 2,