1115951-84-2

Basic information

• Product Name: 2-(2-bromophenyl)-N,N-dimethyl-2-oxoacetamide
• Synonyms: 2-(2-bromophenyl)-N,N-dimethyl-2-oxoacetamide
• CAS NO: 1115951-84-2
• Molecular Weight: 256.099
• Mol File: 1115951-84-2.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: 2-(2-bromophenyl)-N,N-dimethyl-2-oxoacetamide(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2-bromophenyl)-N,N-dimethyl-2-oxoacetamide(1115951-84-2)
• EPA Substance Registry System: 2-(2-bromophenyl)-N,N-dimethyl-2-oxoacetamide(1115951-84-2)

Safety Data

• Hazardous Substances Data: 1115951-84-2(Hazardous Substances Data)

Upstream product

• 951163-93-2 α,α-dibromo-2'-bromoacetophenone 
• 124-40-3 dimethyl amine 
• 2142-69-0 2-bromophenyl methyl ketone 
• 68-12-2 N,N-dimethyl-formamide 
• 26767-16-8 2-(2-bromophenyl)-2-oxoacetic acid 
• 1973-22-4 1-bromo-2-ethylbenzene 
• 680-31-9 N,N,N,N,N,N-hexamethylphosphoric triamide 
• 159749-30-1 1-(2-bromophenyl)-3-(dimethylamino)-2-propen-1-one 

Relevant articles and documents

Metal-Free C=C Double Bond Cleavage on Enaminones for the Synthesis of α-Ketoamides by Free-Radical Aerobic Oxygenation

The tandem oxidation of the enaminone C=C double bond as well as subsequent C-N bond formation are realized under metal-free conditions by thermo-induced free radical transformation. In the presence of benzoyl peroxide (BPO) and N-iodosuccinimide (NIS), a

The syntheses of α-ketoamides vianBu4NI- catalyzed multiple sp3C-H bond oxidation of ethylarenes and sequential coupling with dialkylformamides

The nBu4NI-catalyzed sequential C-O and C-N bond formation via multiple sp3C-H bond activation of ethylarenes, using N,N-dialkylformamide as the amino source, provided α-ketoamides with moderate yields. This journal is

Cu(ii)-catalyzed decarboxylative acylation of acyl C-H of formamides with α-oxocarboxylic acids leading to α-ketoamides

CuBr2-catalyzed decarboxylative acylation of the acyl C-H of N-monosubstituted and N,N-disubstituted formamides with α-oxocarboxylic acids leading to α-ketoamides was developed, which generated the corresponding products in good yields. The Royal Society of Chemistry 2013.