280783-58-6

Basic information

• Product Name: 1H-Azepine-3,4,5,6-tetrol, 1-acetylhexahydro-, tetraacetate (ester), (3R,4R,5R,6R)-
• Synonyms: 1H-Azepine-3,4,5,6-tetrol, 1-acetylhexahydro-, tetraacetate (ester), (3R,4R,5R,6R)-
• CAS NO: 280783-58-6
• Molecular Formula: C16H23 N O9
• Molecular Weight: 373.36
• Mol File: 280783-58-6.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1H-Azepine-3,4,5,6-tetrol, 1-acetylhexahydro-, tetraacetate (ester), (3R,4R,5R,6R)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Azepine-3,4,5,6-tetrol, 1-acetylhexahydro-, tetraacetate (ester), (3R,4R,5R,6R)-(280783-58-6)
• EPA Substance Registry System: 1H-Azepine-3,4,5,6-tetrol, 1-acetylhexahydro-, tetraacetate (ester), (3R,4R,5R,6R)-(280783-58-6)

Safety Data

• Hazardous Substances Data: 280783-58-6(Hazardous Substances Data)

Upstream product

• 108-24-7 acetic anhydride 
• 178964-40-4 1,6-dideoxy-1,6-imino-D-mannitol 

Relevant articles and documents

Short practical synthesis of (3R,4R,5R,6A)-tetrahydroxyazepane and (3S,4S,5S,6S)-trahydroxyazepane from D- And L-chiroinositol, respectively

The polyhydroxylated azepanes (3R,4R,5R,6R)-tetrahydroxyazepane (-)-l and (35,45,5S,65)-tetrahydroxyazepane (+)-1 are synthesised from D-and L-c/j/ro-inositol, respectively. Key transformations in the reaction sequence include a glycol-fission reaction wi