1432744-80-3

Basic information

• Product Name: 1-(p-bromophenyl)prop-2-ynyl 4,6-di-O-acetyl-2,3-dideoxy-β-D-erythro-hex-2-enopyranoside
• Synonyms: 1-(p-bromophenyl)prop-2-ynyl 4,6-di-O-acetyl-2,3-dideoxy-β-D-erythro-hex-2-enopyranoside
• CAS NO: 1432744-80-3
• Molecular Weight: 423.26
• Mol File: 1432744-80-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1-(p-bromophenyl)prop-2-ynyl 4,6-di-O-acetyl-2,3-dideoxy-β-D-erythro-hex-2-enopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(p-bromophenyl)prop-2-ynyl 4,6-di-O-acetyl-2,3-dideoxy-β-D-erythro-hex-2-enopyranoside(1432744-80-3)
• EPA Substance Registry System: 1-(p-bromophenyl)prop-2-ynyl 4,6-di-O-acetyl-2,3-dideoxy-β-D-erythro-hex-2-enopyranoside(1432744-80-3)

Safety Data

• Hazardous Substances Data: 1432744-80-3(Hazardous Substances Data)

Upstream product

• 85020-75-3 1-(4-bromophenyl)-2-propyn-1-ol 
• 2873-29-2 D-glucal triacetate 

Relevant articles and documents

An efficient procedure for the synthesis of 2,3-unsaturated-O-glycosides: TiCl3(OTf) as the catalyst for type i Ferrier rearrangement

An efficient type I Ferrier rearrangement reaction system for the synthesis of 2,3-unsaturated-O-glycosides has been established by using TiCl 3(OTf) as the catalyst. A series of 2,3-unsaturated-O-glucosides were prepared from 3,4,6-tri-O-acetyl-d-glucal in good yield and high anomeric selectivity.