30572-03-3

Basic information

• Product Name: 1,2,4,6-tetra-O-benzoyl-3-O-chloroacetyl-β-D-glucopyranoside
• Synonyms: 1,2,4,6-tetra-O-benzoyl-3-O-chloroacetyl-β-D-glucopyranoside
• CAS NO: 30572-03-3
• Molecular Weight: 673.073
• Mol File: 30572-03-3.mol

Chemical Properties

• CAS DataBase Reference: 1,2,4,6-tetra-O-benzoyl-3-O-chloroacetyl-β-D-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2,4,6-tetra-O-benzoyl-3-O-chloroacetyl-β-D-glucopyranoside(30572-03-3)
• EPA Substance Registry System: 1,2,4,6-tetra-O-benzoyl-3-O-chloroacetyl-β-D-glucopyranoside(30572-03-3)

Safety Data

• Hazardous Substances Data: 30572-03-3(Hazardous Substances Data)

Upstream product

• 72076-17-6 1,2,4,6-tetra-O-benzoyl-β-D-glucopyranoside 
• 541-88-8 Chloroacetic anhydride 

Downstream Products

• 138857-85-9 1,2,3-tri-O-benzoyl-4,6-O-<(R)-1-methoxycarbonyl(ethylidene)>-α-D-galactopyranose 
• 195063-73-1 benzyl 2,4,6-tri-O-benzoyl-β-D-glucopyranoside 
• 195063-72-0 benzyl 2,4,6-tri-O-benzoyl-3-O-chloroacetyl-β-D-glucopyranoside 
• 195063-76-4 benzyl O-(2,4,6-tri-O-benzoyl-β-D-glucopyranosyl)-(1->3)-2-O-benzoyl-4,6-O-<(S)-1-methoxycarbonyl(ethylidene)>-α-D-glucopyranoside 
• 195063-75-3 (2S,4aR,6S,7R,8S,8aR)-7-Benzoyloxy-6-benzyloxy-8-[(2S,3R,4S,5R,6R)-3,5-bis-benzoyloxy-6-benzoyloxymethyl-4-(2-chloro-acetoxy)-tetrahydro-pyran-2-yloxy]-2-methyl-hexahydro-pyrano[3,2-d][1,3]dioxine-2-carboxylic acid methyl ester 
• 195063-79-7 O-{2,3-di-O-benzoyl-4,6-O-[(R)-1-methoxycarbonyl(ethylidene)]-α-D-galactopyranosyl}-(1->3)-2,4,6-tri-O-benzoyl-β-D-glucopyranosyl-(1->3)-2-O-benzoyl-4,6-O-[(S)-1-methoxycarbonyl(ethylidene)]-α-D-glucopyranose 
• 195063-71-9 2,4,6-tri-O-benzoyl-3-O-chloroacetyl-α-D-glucopyranosyl bromide 

Relevant articles and documents

Unusual reactivity of pyruvated glycosyl donors during construction of rhizobial exopolysaccharide fragments

Two pyruvated galactosyl donors, 2,3-di-O-benzoyl-4,6-0-[1-(R)-methoxycarbonyl(ethylidene)]-α-D- galactopyranosyl chloride (6) and trichloroacetimidate 13, were coupled to position 3 of suitably protected mono and disaccharide benzyl glucoside acceptors. For both donors, an unusual high content of the α-(1→3)-linked products was obtained. The corresponding β-(1→3)-linked di- and trisaccharides are related to exopolysaccharides of Rhizobium leguminosarum.