1437303-53-1

Basic information

• Product Name: ethyl 3,4-di-O-benzyl-2-O-(p-methoxybenzyl)-1-thio-α-L-rhamnoside
• Synonyms: ethyl 3,4-di-O-benzyl-2-O-(p-methoxybenzyl)-1-thio-α-L-rhamnoside
• CAS NO: 1437303-53-1
• Molecular Weight: 508.679
• Mol File: 1437303-53-1.mol

Chemical Properties

• CAS DataBase Reference: ethyl 3,4-di-O-benzyl-2-O-(p-methoxybenzyl)-1-thio-α-L-rhamnoside(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 3,4-di-O-benzyl-2-O-(p-methoxybenzyl)-1-thio-α-L-rhamnoside(1437303-53-1)
• EPA Substance Registry System: ethyl 3,4-di-O-benzyl-2-O-(p-methoxybenzyl)-1-thio-α-L-rhamnoside(1437303-53-1)

Safety Data

• Hazardous Substances Data: 1437303-53-1(Hazardous Substances Data)

Upstream product

• 130847-19-7 ethyl 3,4-di-O-benzyl-1-thio-α-L-rhamnopyranoside 
• 824-94-2 p-methoxybenzyl chloride 

Downstream Products

• 1437303-55-3 phenyl [3,4-di-O-benzyl-2-O-(p-methoxybenzyl)-α-L-rhamnopyranosyl]-(1→3)-2,3,6-tri-benzoyl-1-thio-β-D-glucopyranoside 

Relevant articles and documents

Facile synthesis of a pentasaccharide repeating unit corresponding to the common O-antigen of Salmonella enterica O57 and Escherichia coli O51

A concise chemical synthetic strategy has been developed for the synthesis of a pentasaccharide present in the O-antigen of Salmonella enterica O57 and Escherichia coli O51 strains. A sequential glycosylation strategy has been adopted for the synthesis of the target pentasaccharide. All intermediate steps are high yielding and the glycosylation steps are stereoselective. A number of recently developed methodologies have been used in the synthesis.