104343-33-1

Basic information

• Product Name: 7-O-BETA-D-GLUCOPYRANOSYL-ALPHA-HOMONOJIRIMYCIN
• Synonyms: 7-O-BETA-D-GLUCOPYRANOSYL-ALPHA-HOMONOJIRIMYCIN;MDL 25637;(2R)-2α-[(β-D-Glucopyranosyloxy)methyl]-6β-(hydroxymethyl)-3α,4β,5α-piperidinetriol;7-O-Glucosyl-α-homonojirimycin;7-O-β-D-Glucopyranosyl-2,6-dideoxy-2,6-epimino-D-glycero-L-gulo-heptitol;7-O-β-D-Glucopyranosyl-α-homonojirimycin
• CAS NO: 104343-33-1
• Molecular Formula: C13H25NO10
• Molecular Weight: 355.34
• Mol File: 104343-33-1.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 652.7°C at 760 mmHg
• Flash Point: 348.6°C
• Appearance: /
• Density: 1.68g/cm³
• Vapor Pressure: 8.4E-20mmHg at 25°C
• Refractive Index: 1.654
• CAS DataBase Reference: 7-O-BETA-D-GLUCOPYRANOSYL-ALPHA-HOMONOJIRIMYCIN(CAS DataBase Reference)
• NIST Chemistry Reference: 7-O-BETA-D-GLUCOPYRANOSYL-ALPHA-HOMONOJIRIMYCIN(104343-33-1)
• EPA Substance Registry System: 7-O-BETA-D-GLUCOPYRANOSYL-ALPHA-HOMONOJIRIMYCIN(104343-33-1)

Safety Data

• Hazardous Substances Data: 104343-33-1(Hazardous Substances Data)

Usage

InChI:InChI=1/C13H25NO10/c1-23-13(12(22)10(21)7(18)5(3-16)24-13)11-9(20)8(19)6(17)4(2-15)14-11/h4-12,14-22H,2-3H2,1H3/t4-,5-,6-,7-,8+,9-,10+,11?,12-,13-/m1/s1

Upstream product

• 120172-80-7 2,6-dideoxy-2,6-imino-D-glycero-L-gulo-heptitol 1,3,4,5-tetrabenzoate hydrochloride 
• 120172-79-4 2,6-dideoxy-2,6-(trifluoroacetimido)-D-glycero-D-ido-heptonic acid 3,4,5,7-tetrabenzoate 
• 120172-78-3 2,6-dideoxy-2,6-(trifluoroacetimido)-D-glycero-D-ido-heptononitrile 3,4,5,7-tetrabenzoate 
• 120172-81-8 2,6-dideoxy-2,6-<<(phenylmethoxy)carbonyl>imino>-D-glycero-L-gulo-heptitol 1,3,4,5-tetrabenzoate 
• 120172-77-2 2,6-dideoxy-2,6-imino-D-glycero-D-ido-heptononitrile 3,4,5,7-tetrabenzoate 
• 78821-34-8 2,6-dideoxy-2,6-imino-D-glycero-D-ido-heptononitrile 
• 74808-10-9 O-(2,3,4,6-Tetra-O-acetyl-α-D-glucopyranosyl)trichloroacetimidate 
• 104343-35-3 2,6-dideoxy-2,6-<<(phenylmethoxy)carbonyl>imino>-7-O-<2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl>-1,3,4,5-tetrakis-O-(phenylmethyl)-D-glycero-L-gulo-hepitol 
• 104343-30-8 1,2,6-trideoxy-6-<<(phenylmethoxy)carbonyl>amino>-3,4,5,7-tetrakis-O-(phenylmethyl)-D-gluco-hept-1-enitol 
• 104343-31-9 2,6-dideoxy-2,6-<<(phenylmethoxy)carbonyl>imino>-1,3,4,5-tetrakis-O-(phenylmethyl)-D-glycero-L-gulo-heptitol 
• 4196-35-4 2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl bromide 
• 104343-32-0 2,6-dideoxy-2,6-<<(phenylmethoxy)carbonyl>imino>-7-O-<2,3,4,6-tetrakis-O-(phenylmethyl)-β-D-glucopyranosyl>-1,3,4,5-tetrakis-O-(phenylmethyl)-D-glycero-L-gulo-hepitol 
• 120204-12-8 2,6-dideoxy-2,6-<<(phenylmethoxy)carbonyl>imino>-7-O-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-D-glycero-L-gulo-heptitol 1,3,4,5-tetrabenzoate 

Relevant articles and documents

Process for hydrolyzing 2,6-dideoxy-2,6-iminoheptononitrile derivatives using trifluoroacetic acid and dinitrogen tetroxide

A procedure for the mild conversion of a carbonitrile to the corresponding carboxylic acid by first using trifluoroacetic acid in the presence of a catalytic amount of mercuric ion followed by oxidative hydrolysis with dinitrogen tetroxide is described herein. The use of this procedure in the preparation of 1,3,4,5-tetra-O-benzoyl-2,6-dideoxy-2,6-imino-D-glycero-L-gulo-heptitol hydrochloride is also described here.

Total synthesis of 2,6-dideoxy-2,6-imino-7-O-β-D-glucopyranosyl-D-glycero-L-gulo-heptitol hydrochloride: A potent inhibitor of α-glucosidases

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