939989-89-6

Basic information

• Product Name: 2-(2'-bromophenyl)-5-methyloxazole
• Synonyms: 2-(2'-bromophenyl)-5-methyloxazole
• CAS NO: 939989-89-6
• Molecular Weight: 238.084
• Mol File: 939989-89-6.mol

Chemical Properties

• CAS DataBase Reference: 2-(2'-bromophenyl)-5-methyloxazole(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2'-bromophenyl)-5-methyloxazole(939989-89-6)
• EPA Substance Registry System: 2-(2'-bromophenyl)-5-methyloxazole(939989-89-6)

Safety Data

• Hazardous Substances Data: 939989-89-6(Hazardous Substances Data)

Upstream product

• 1016705-85-3 2-bromo-N-(prop-2-yn-1-yl)benzamide 
• 4001-73-4 2-Bromobenzamide 
• 513-31-5 2-bromoallyl bromide 
• 7154-66-7 2-bromobenzoic acid chloride 

Relevant articles and documents

A facile one-pot synthesis of 2-o-cyanoaryl oxazole derivatives mediated by CuCN

A convenient, inexpensive and effective approach to the synthesis of 2-o-cyanoaryl oxazole derivatives has been developed. Generally, the copper-mediated cyclization/coupling reactions afforded corresponding 2-cyanoaryl oxazoles and oxazolines in moderate

Base-Promoted Cycloisomerization for the Synthesis of Oxazoles and Imidazoles

Treatment of propargylamides or propargylamidines with cesium carbonate in DMSO results in the formation of the corresponding oxazoles or imidazoles in good yields. A large variety of substrates with various functional groups are tolerated. DFT study on a model substrate reveals that the reactions proceed via a sequence involving allene formation, intramolecular cyclization, and double-bond isomerization.

Facile, selective, and regiocontrolled synthesis of oxazolines and oxazoles mediated by ZnI2 and FeCl3

An expedient method for a direct approach to the selective and regiocontrolled synthesis of 2-oxazolines and 2-oxazoles mediated by ZnI 2 and FeCl3 is described. A Lewis acid promoted cyclization of acetylenic amide with various func

A simple one-pot synthesis of 2-aryl-5-alkyl-Substituted oxazoles byCs 2CO3-Mediated Reactions of aromatic primary amides with 2,3-dibromopropene

A simple and efficient method for the synthesis of 2-aryl-5-alkyl- substituted oxazoles has been developed. A series of 2,5-disubstituted oxazoles were synthesized in a single step by Cs2CO3-mediated reactions of aromatic primary amides with 2,3-dibromopr