1239713-17-7

Basic information

• Product Name: 2-(4-bromophenyl)-5-phenyl-4,5-dihydro-1,3-oxazole
• Synonyms: 2-(4-bromophenyl)-5-phenyl-4,5-dihydro-1,3-oxazole
• CAS NO: 1239713-17-7
• Molecular Weight: 302.17
• Mol File: 1239713-17-7.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2-(4-bromophenyl)-5-phenyl-4,5-dihydro-1,3-oxazole(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4-bromophenyl)-5-phenyl-4,5-dihydro-1,3-oxazole(1239713-17-7)
• EPA Substance Registry System: 2-(4-bromophenyl)-5-phenyl-4,5-dihydro-1,3-oxazole(1239713-17-7)

Safety Data

• Hazardous Substances Data: 1239713-17-7(Hazardous Substances Data)

Upstream product

• 328931-56-2 4-bromo-N-(2-phenylethyl)benzamide 

Downstream Products

• 1239713-01-9 4-bromo-N-(2-(1H-imidazol-1-yl)-2-phenylethyl)benzamide 

Relevant articles and documents

Visible light bromide catalysis for oxazoline, pyrrolidine, and dihydrooxazine synthesesviaCsp3-H functionalizations

A catalytic benzylic Csp3-H functionalization protocol is described here. This visible light-mediated process is centered on the utilization of a bromide catalyst and oxidant to generate a nitrogen (N)-centered radical for a site-selective hydrogen atom transfer (HAT) process. This strategy enabled the unconventional syntheses of a number of N-heterocycles dependent on the amide identity. We also discovered a nucleophilicity-dependent kinetic resolution for stereochemical differentiation of Csp3-H bonds that enabled the stereoselective synthesis ofcis- andtrans-oxazolines.