284031-35-2

Basic information

• Product Name: 1H-Azepine-3,4,6-triol, hexahydro-, (3R,4S,6R)- (9CI)
• Synonyms: 1H-Azepine-3,4,6-triol, hexahydro-, (3R,4S,6R)- (9CI)
• CAS NO: 284031-35-2
• Molecular Formula: C6H13NO3
• Molecular Weight: 147.17232
• Product Categories: ALCOHOL
• Mol File: 284031-35-2.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1H-Azepine-3,4,6-triol, hexahydro-, (3R,4S,6R)- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Azepine-3,4,6-triol, hexahydro-, (3R,4S,6R)- (9CI)(284031-35-2)
• EPA Substance Registry System: 1H-Azepine-3,4,6-triol, hexahydro-, (3R,4S,6R)- (9CI)(284031-35-2)

Safety Data

• Hazardous Substances Data: 284031-35-2(Hazardous Substances Data)

Upstream product

• 284031-27-2 3-deoxy-1,2-O-isopropylidene-α-L-xylo-hexofuranose 
• 284031-29-4 3-deoxy-1,2-O-isopropylidene-6-O-tosyl-α-L-xylo-hexofuranose 
• 943032-32-4 C₁₉H₂₈O₇ 
• 943032-33-5 (3R,4R,6S)-1-benzyl-6-O-benzyl-3,4,6-trihydroxy-3,4-[(2S,3S)-2,3-dimethoxybutane-2,3-dioxy]azepane 
• 284031-25-0 3-deoxy-1,2:5,6-di-O-isopropylidene-α-L-xylo-hexofuranose 
• 79645-44-6 3-deoxy-L-xylo-hexono-1,4-lactone 
• 284031-31-8 6-azido-3,6-dideoxy-1,2-O-isopropylidene-α-L-xylo-hexofuranose 
• 4613-62-1 3-deoxy-1,2;5,6-di-O-isopropylidene-α-D-glucofuranoside 
• 58475-16-4 [(2R)-2-[(3aR,5S,6aR)-2,2-dimethyl-3a,5,6,6a-tetrahydrofuro[2,3-d] [1,3]dioxol-5-yl]-2-hydroxy-ethyl]4-methylbenzenesulfonate 
• 284031-17-0 (R)-2-azido-1-((3aR,5S,6aR)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-5-yl)ethan-1-ol 
• 2774-29-0 (3aR,5R,6aR)-5-[(4R)-2,2-dimethyl-1,3-dioxolan-4-yl]-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxole 
• 6936-66-9 3-deoxy-D-xylo-hexono-1,4-lactone 
• 162427-40-9 3-deoxygalactose (α-furanose) 
• 22323-55-3 3-deoxy-1,2-O-isopropylidene-6-O-tosyl-α-D-xylo-hexofuranose 

Relevant articles and documents

Expeditious synthesis of tri- and tetrahydroxyazepanes from D-(-)-quinic acid as potent glycosidase inhibitors

(Chemical Equation Presented) Several new stereoisomers of 3,4,6-trihydroxyazepanes and 7-hydroxymethyl-3,4,5-trihydroxyazepanes as well as known 3,4,5-trihydroxyazepanes were synthesized as potent glycosidase inhibitors from D-(-)-quinic acid in an effic

Syntheses of sugar-related trihydroxyazepanes from simple carbohydrates and their activities as reversible glycosidase inhibitors

Five diastereomeric trideoxy-1,6-iminohexitols were synthesised, and their inhibitory activities were determined against selected glycosidases. For comparison, 1,4,5-trideoxy-1,5-imino-D-lyxo-hexitol, the 4-deoxy derivative of 1-deoxymannojirimicin, was prepared by enzymatic isomerisation of 6-azido-3,6-dideoxy-D-ribo-hexose into the corresponding 2-ulose and subsequent hydrogenation accompanied by intramolecular reductive amination. (C) 2000 Elsevier Science Ltd.