1384525-54-5

Basic information

• Product Name: (3R,4S,5R,6S)-N-benzyloxycarbonyl-3-hydroxy-3-methyl-4,5,6-tribenzyloxyazepane
• Synonyms: (3R,4S,5R,6S)-N-benzyloxycarbonyl-3-hydroxy-3-methyl-4,5,6-tribenzyloxyazepane
• CAS NO: 1384525-54-5
• Molecular Weight: 581.709
• Mol File: 1384525-54-5.mol

Chemical Properties

• CAS DataBase Reference: (3R,4S,5R,6S)-N-benzyloxycarbonyl-3-hydroxy-3-methyl-4,5,6-tribenzyloxyazepane(CAS DataBase Reference)
• NIST Chemistry Reference: (3R,4S,5R,6S)-N-benzyloxycarbonyl-3-hydroxy-3-methyl-4,5,6-tribenzyloxyazepane(1384525-54-5)
• EPA Substance Registry System: (3R,4S,5R,6S)-N-benzyloxycarbonyl-3-hydroxy-3-methyl-4,5,6-tribenzyloxyazepane(1384525-54-5)

Safety Data

• Hazardous Substances Data: 1384525-54-5(Hazardous Substances Data)

Upstream product

• 1384525-50-1 C₃₆H₃₉NO₇ 

Relevant articles and documents

Synthesis of branched seven-membered 1-N-iminosugars and their evaluation as glycosidase inhibitors

Four branched tetra- and pentahydroxylated azepanes have been synthesized from a common azepane precursor through dihydroxylation followed by deoxygenation. They have been assayed as glycosidase inhibitors on a panel of 22 glycosidases and one methylated azepane displayed selective, competitive, and moderate inhibition toward bovine kidney α-l-fucosidase.