146537-22-6

Basic information

• Product Name: 2-((4-chlorophenyl)amino)-1-(4-fluorophenyl)ethanone
• Synonyms: 2-((4-chlorophenyl)amino)-1-(4-fluorophenyl)ethanone
• CAS NO: 146537-22-6
• Molecular Weight: 263.699
• Mol File: 146537-22-6.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2-((4-chlorophenyl)amino)-1-(4-fluorophenyl)ethanone(CAS DataBase Reference)
• NIST Chemistry Reference: 2-((4-chlorophenyl)amino)-1-(4-fluorophenyl)ethanone(146537-22-6)
• EPA Substance Registry System: 2-((4-chlorophenyl)amino)-1-(4-fluorophenyl)ethanone(146537-22-6)

Safety Data

• Hazardous Substances Data: 146537-22-6(Hazardous Substances Data)

Upstream product

• 106-47-8 4-chloro-aniline 
• 403-29-2 2-bromo-4'-fluoroacetophenone 

Downstream Products

• 76609-16-0 5-chloro-2-(4-fluorophenyl)-1H-indole 
• 146537-37-3 1-(4-Chloro-phenyl)-4-(4-fluoro-phenyl)-2-methyl-1H-pyrrole-3-carboxylic acid ethyl ester 

Relevant articles and documents

Regioselective Synthesis of 2-Arylindoles via Palladium-Catalyzed Cyclization of Phenylglyoxal and 2-Anilinoacetophenones with Anilines

A versatile route has been developed for the synthesis of 2-arylindoles using a Pd-catalyzed tandem process. Under reductive conditions, different 2-arylindoles were synthesized from phenylglyoxal and aniline. This synthetic methodology involves a tandem reaction of four steps with high regioselectivity. Alternatively, 2-anilinoacetophenones intermediates also can be using to give access to the corresponding 2-arylindoles.