79110-04-6

Basic information

• Product Name: 1-(2-((4-nitrophenyl)amino)phenyl)ethanone
• Synonyms: 1-(2-((4-nitrophenyl)amino)phenyl)ethanone
• CAS NO: 79110-04-6
• Molecular Weight: 256.261
• Mol File: 79110-04-6.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 1-(2-((4-nitrophenyl)amino)phenyl)ethanone(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(2-((4-nitrophenyl)amino)phenyl)ethanone(79110-04-6)
• EPA Substance Registry System: 1-(2-((4-nitrophenyl)amino)phenyl)ethanone(79110-04-6)

Safety Data

• Hazardous Substances Data: 79110-04-6(Hazardous Substances Data)

Upstream product

• 551-93-9 2-aminoacetophenone 
• 586-78-7 para-nitrophenyl bromide 
• 98-95-3 nitrobenzene 
• 636-98-6 p-nitrobenzene iodide 

Downstream Products

• 1246849-45-5 (E)-1-(2-(4-nitrophenylamino)phenyl)ethanone oxime 
• 130266-47-6 1-(4-nitrophenyl)indoline-2,3-dione 

Relevant articles and documents

Divergent strategy for the chemoselective synthesis of N-Arylbenzimidazoles and N-Arylindazoles from arylamino oximes

An efficient and divergent synthesis of N-arylbenzimidazoles and N-arylindazoles from arylamino oximes based on reaction conditions selection was developed. The synthesis was approached by treating oximes with BTC and the chemoselectivity was regulated by the amount of Et3N. This switchable N–N and N–C bond formation process features mild reaction conditions, simple execution, high chemoselectivity and broad substrate scope.

Copper-catalyzed intramolecular oxidative C(sp3)-H amidation of 2-aminoacetophenones: Efficient synthesis of indoline-2,3-diones

An efficient synthesis of diverse indoline-2,3-diones from 2-aminoacetophenones through copper-catalyzed intramolecular C(sp3)-H amidation is developed. The reaction proceeds in DMSO by using O2 as the sole oxidant to provide the desired products in moderate to good yields.

The Preparation of Some 2-Nitroacridines and Related Compounds

The reaction of 2-fluoro-5-nitrobenzaldehyde with a wide variety of arylamines gives, in general, mixtures of the corresponding 2-arylamino-5-nitrobenzaldehydes and their related anils.Both aldehydes and anils readily underwent acid-catalysed cyclization to give the corresponding 2-nitroacridines.The effect of substituent on the rate of cyclization of these aldehydes and of some related anilino-benzaldehydes and -acetophenones has been studied in trifluoroacetic acid solution by means of 1H n.m.r. spectroscopy.A solution of 2-(N-methylanilino)-5-nitrobenzaldehydein trifluoroacetic acid appears to contain a substituted acridinium ion; treatment of this solution with alkali gave 10-methyl-2-nitroacridone. 1H n.m.r. data for a wide variety of substituted 2-nitroacridines are discussed.