1415639-03-0

Basic information

• Product Name: 1-O-(3′-iodophenyl)-2,3,4,6-tetra-O-acetyl-α-D-glucopyranoside
• Synonyms: 1-O-(3′-iodophenyl)-2,3,4,6-tetra-O-acetyl-α-D-glucopyranoside
• CAS NO: 1415639-03-0
• Molecular Weight: 550.301
• Mol File: 1415639-03-0.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1-O-(3′-iodophenyl)-2,3,4,6-tetra-O-acetyl-α-D-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: 1-O-(3′-iodophenyl)-2,3,4,6-tetra-O-acetyl-α-D-glucopyranoside(1415639-03-0)
• EPA Substance Registry System: 1-O-(3′-iodophenyl)-2,3,4,6-tetra-O-acetyl-α-D-glucopyranoside(1415639-03-0)

Safety Data

• Hazardous Substances Data: 1415639-03-0(Hazardous Substances Data)

Upstream product

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

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.