903881-57-2

Basic information

• Product Name: 1-O-(3′-iodophenyl)-2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside
• Synonyms: 1-O-(3′-iodophenyl)-2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside
• CAS NO: 903881-57-2
• Molecular Weight: 550.301
• Mol File: 903881-57-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1-O-(3′-iodophenyl)-2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: 1-O-(3′-iodophenyl)-2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside(903881-57-2)
• EPA Substance Registry System: 1-O-(3′-iodophenyl)-2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside(903881-57-2)

Safety Data

• Hazardous Substances Data: 903881-57-2(Hazardous Substances Data)

Upstream product

• 3947-62-4 2,3,4,5-tetra-O-acetyl-D-glucopyranose 
• 221037-98-5 (3-iodophenyl)boronic acid 
• 626-02-8 3-Iodophenol 
• 74808-10-9 2,3,4,6-tetra-O-acetyl-d-glucopyranosyl trichloroacetimidate 
• 604-69-3 β-D-glucose pentaacetate 

Downstream Products

• 903881-53-8 4-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-3'-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)biphenyl 

Relevant articles and documents

Copper-Catalyzed Anomeric O-Arylation of Carbohydrate Derivatives at Room Temperature

Direct and practical anomeric O-arylation of sugar lactols with substituted arylboronic acids has been established. Using copper catalysis at room temperature under an air atmosphere, the protocol proved to be general, and a variety of aryl O-glycosides have been prepared in good to excellent yields. Furthermore, this approach was extended successfully to unprotected carbohydrates, including α-mannose, and it was demonstrated here how the interaction between carbohydrates and boronic acids can be combined with copper catalysis to achieve selective anomeric O-arylation.

Antagonists of the myelin-associated glycoprotein: A new class of tetrasaccharide mimics

The tetrasaccharide substructure 1 of the ganglioside GQ1bα shows a remarkable affinity for the myelin-associated glycoprotein (MAG). In the search for structurally simplified and pharmacokinetically improved mimics of 1, biphenyl was identified as a feas