1453084-69-9

Basic information

• Product Name: (2R,3R,4S,5R,6R)-2-(acetoxymethyl)-6-((4-iodophenyl)amino)tetrahydro-2H-pyran-3,4,5-triyl triacetate
• Synonyms: (2R,3R,4S,5R,6R)-2-(acetoxymethyl)-6-((4-iodophenyl)amino)tetrahydro-2H-pyran-3,4,5-triyl triacetate
• CAS NO: 1453084-69-9
• Molecular Weight: 549.316
• Mol File: 1453084-69-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (2R,3R,4S,5R,6R)-2-(acetoxymethyl)-6-((4-iodophenyl)amino)tetrahydro-2H-pyran-3,4,5-triyl triacetate(CAS DataBase Reference)
• NIST Chemistry Reference: (2R,3R,4S,5R,6R)-2-(acetoxymethyl)-6-((4-iodophenyl)amino)tetrahydro-2H-pyran-3,4,5-triyl triacetate(1453084-69-9)
• EPA Substance Registry System: (2R,3R,4S,5R,6R)-2-(acetoxymethyl)-6-((4-iodophenyl)amino)tetrahydro-2H-pyran-3,4,5-triyl triacetate(1453084-69-9)

Safety Data

• Hazardous Substances Data: 1453084-69-9(Hazardous Substances Data)

Upstream product

• 41355-50-4 2,3,4,6-tetra-O-acetyl-D-glucosyl-1-amine 
• 5122-99-6 4-iodophenylboronic acid 

Relevant articles and documents

Stereoselective copper-catalyzed Chan-Lam-Evans N-arylation of glucosamines with arylboronic acids at room temperature

An efficient and practical N-arylation of glycosylamines with substituted aryl boronic acids has been established. Using Cu(OAc)2 and pyridine at room temperature under air atmosphere, the protocol proved to be general, and a variety of aryl N-glycosides have been prepared in good to excellent yields with exclusive β selectivity.