1000775-45-0

Basic information

• Product Name: N,N-bis(phenacyl)-4-chloroaniline
• Synonyms: N,N-bis(phenacyl)-4-chloroaniline
• CAS NO: 1000775-45-0
• Molecular Weight: 363.843
• Mol File: 1000775-45-0.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: N,N-bis(phenacyl)-4-chloroaniline(CAS DataBase Reference)
• NIST Chemistry Reference: N,N-bis(phenacyl)-4-chloroaniline(1000775-45-0)
• EPA Substance Registry System: N,N-bis(phenacyl)-4-chloroaniline(1000775-45-0)

Safety Data

• Hazardous Substances Data: 1000775-45-0(Hazardous Substances Data)

Upstream product

• 106-47-8 4-chloro-aniline 
• 70-11-1 α-bromoacetophenone 
• 98-86-2 acetophenone 

Downstream Products

• 113523-84-5 2-(4-chlorophenylamino)-1,4-diphenylbut-2-ene-1,4-dione 
• 1446221-41-5 2,6-bisphenyl-4-(4-chlorophenyl)-4H-1,4-oxazine 
• 36004-55-4 (5-chloro-3-phenyl-1H-indol-2-yl)(phenyl)methanone 
• 106-47-8 4-chloro-aniline 
• 36004-54-3 phenyl(3-phenyl-1H-indol-2-yl)methanone 
• 853-37-2 1-(4-chlorophenyl)-2,5-diphenyl-1H-pyrrole 
• 60532-59-4 1-(4-chlorophenyl)-3,4-diphenyl-1H-pyrrole 
• 859157-97-4 1-(4-chlorophenyl)-3,4-diphenyl-2,5-dihydro-1H-pyrrole 
• 54951-51-8 1,4-bis(4-chlorophenyl)-2,6-diphenyl-1,4-dihydropyrazine 

Relevant articles and documents

Ultrasound-mediated synthesis of N,N-bis(phenacyl)aniline under solvent-free conditions

An efficient method for the synthesis of N,N-bis(phenacyl)anilines was developed via smooth condensation of anilines with α-bromoacetophenones in the presence of sodium carbonate as acid acceptor and polyethylene glycol 400 (PEG 400) as catalyst at room t

Synthesis of 4H-1,4-oxazines as transthyretin amyloid fibril inhibitors

4H-1,4-oxazines were designed as transthyretin (TTR) amyloid fibril inhibitors based on an analysis of the interactions between known small molecule inhibitors and TTR by molecular docking. A series of 2,4,6-triaryl-4H-1,4- oxazines was synthesized by the

Study on photochromism of diarylethenes with a 2,5-dihydropyrrole bridging unit: A convenient preparation of 3,4-diarylpyrroles from 3,4-diaryl-2,5- dihydropyrroles

Symmetric and nonsymmetric diarylethenes with a 2,5-dihydropyrrole bridging unit have been prepared, and the photochromic properties are investigated. Both symmetric and nonsymmetric diarylethenes with 2,5-dihydropyrrole bridging units undergo reversible ring-opening and ring-closing photoisomerization reactions in nonpolar solvents with UV/vis light, and some of them exhibit good fatigue resistance and no marked degradation detected after 10 cycles via an on/off switch. In polar solvents, however, photochromic diarylethenes with 2,5-dihydropyrrole bridging units produce 3,4-diarylpyrrole derivatives instead of the ring-closing isomer of diarylethenes with UV light irradiation. A class of N-substituted 3,4-diphenylethenes with 2,5-dihydropyrrole bridging units were prepared and used as templates to investigate the conversion reactions. The mechanism of photoconversion of 3,4-diaryl-2,5-dihydropyrroles to 3,4-diarylpyrroles was explored as well.