89756-10-5

Basic information

• Product Name: benzyl 3,4-di-O-benzoyl-α-L-rhamnopyranoside
• Synonyms: benzyl 3,4-di-O-benzoyl-α-L-rhamnopyranoside
• CAS NO: 89756-10-5
• Molecular Weight: 462.499
• Mol File: 89756-10-5.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: benzyl 3,4-di-O-benzoyl-α-L-rhamnopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: benzyl 3,4-di-O-benzoyl-α-L-rhamnopyranoside(89756-10-5)
• EPA Substance Registry System: benzyl 3,4-di-O-benzoyl-α-L-rhamnopyranoside(89756-10-5)

Safety Data

• Hazardous Substances Data: 89756-10-5(Hazardous Substances Data)

Upstream product

• 89756-07-0 benzyl-2-O-acetyl-3,4-di-O-benzoyl-α-L-rhamnopyranoside 
• 100-51-6 benzyl alcohol 
• 98-88-4 benzoyl chloride 
• 85572-67-4 2-O-acetyl-3,4-di-O-benzoyl-L-rhamnopyranosyl bromide 
• 105285-86-7 benzyl 4-O-benzoyl-2,3-O-isopropylidene-α-L-rhamnopyranoside 
• 3359-35-1 (2R,3R,4R,5R,6S)-2-benzyloxy-tetrahydro-6-methyl-2H-pyran-3,4,5-triol 
• 73-34-7 L-rhamnose 
• 53270-14-7 benzyl 2,3-O-isopropylidene-α-L-rhamnopyranoside 
• 502423-54-3 benzyl 4-O-benzoyl-α-L-rhamnopyranoside 

Downstream Products

• 502423-57-6 benzyl (2,4-di-O-benzoyl-α-L-rhamnopyranosyl)-(1->2)-3,4-di-O-benzoyl-α-L-rhamnopyranoside 
• 502423-56-5 benzyl (2,4-di-O-benzoyl-3-O-chloroacetyl-α-L-rhamnopyranosyl)-(1->2)-3,4-di-O-benzoyl-α-L-rhamnopyranoside 
• 89756-08-1 C₄₉H₄₆O₁₄ 
• 105285-87-8 benzyl 3,4-di-O-benzoyl-2-(2,3,4,6-tetra-O-benzyl-α-D-galactopyranosyl)-α-L-rhamnopyranoside 

Relevant articles and documents

Oligomerization of a rhamnanic trisaccharide repeating unit of O-chain polysaccharides from phytopathogenic bacteria

An efficient synthesis of a protected trisaccharide building block α-L-Rha(1→3)-α-L-Rha(1→2)-α-L-Rha related to the structure of many lipopolysaccharide O-chains from phytopathogenic bacteria has been developed. The protecting group pattern consisting of benzoyl, benzyl and chloroacetyl groups facilitated the use of the trisaccharide building block in the synthesis of two higher oligomers, an oligorhamnosyl hexasaccharide and a nonasaccharide.

SYNTHESIS OF THE PRINCIPAL CHAIN OF THE o-ANTIGENIC POLYSACCARIDES OF Shigella Flexneri. COMMUNICATION 1. SYNTHESIS of 2,4- AND 3,4-DI-o-BENZOYL-α-L-RHAMNOPYRANOSIDES BY A COMBINATION OF SELECTIVE ACYLATION AND DEACETYLATION, AND THE SYNTHESIS OF 1,2-DI-o

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