368452-23-7

Basic information

• Product Name: (2,3-dideoxy-β-D-erythro-hex-2-enopyranosyl)benzene
• Synonyms: (2,3-dideoxy-β-D-erythro-hex-2-enopyranosyl)benzene
• CAS NO: 368452-23-7
• Molecular Weight: 206.241
• Mol File: 368452-23-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (2,3-dideoxy-β-D-erythro-hex-2-enopyranosyl)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: (2,3-dideoxy-β-D-erythro-hex-2-enopyranosyl)benzene(368452-23-7)
• EPA Substance Registry System: (2,3-dideoxy-β-D-erythro-hex-2-enopyranosyl)benzene(368452-23-7)

Safety Data

• Hazardous Substances Data: 368452-23-7(Hazardous Substances Data)

Upstream product

• 201232-87-3 [4,6-di-O-(tert-butyldimethylsilyl)-2,3-dideoxy-β-D-erythro-hex-2-enopyranosyl]benzene 
• 201232-73-7 p-tert-butylphenyl 4,6-di-O-tert-butyl(dimethyl)silyl-2,3-dideoxy-α-D-erythro-hex-2-enopyranoside 

Downstream Products

• 3682-06-2 (2,3,4,6-tetra-O-acetyl-β-D-mannopyranosyl)benzene 
• 891785-95-8 (6-O-tert-butyldimethylsilyl-2,3-dideoxy-β-D-erythro-hex-2-enopyranosyl)benzene 
• 368452-29-3 (2,3-dideoxy-β-D-erythro-hexanopyranosyl)benzene 

Relevant articles and documents

Epoxidation and bis-hydroxylation of C-phenyl-Δ2,3- glycopyranosides

Epoxidation and cis-hydroxylation of C-phenyl-Δ2,3 -glycopyranosides have been carried out with a view to developing C-aryl glycoside synthesis. Epoxidation of (2,3-dideoxy-D-erythro-hex-2-enopyranosyl) benzene and (6-O-tert-butyldimethylsilyl-

Enantiopure trioxadecalin derived liquid crystals: Influence of phenyl substitution on the mesogenic properties

Nickel(0)-catalyzed reaction of pseudo-glucal 1 with Grignard reagents derived from bromobenzene and 1-bromo-4-phenylbenzene gives the corresponding β-C-aryl glycosides 2. Desilylation and hydrogenation of 2 leads to saturated β-C-aryl glycosides 4, which