1246849-42-2

Basic information

• Product Name: (E)-1-(2-(4-fluorophenylamino)phenyl)ethanone oxime
• Synonyms: (E)-1-(2-(4-fluorophenylamino)phenyl)ethanone oxime
• CAS NO: 1246849-42-2
• Molecular Weight: 244.268
• Mol File: 1246849-42-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (E)-1-(2-(4-fluorophenylamino)phenyl)ethanone oxime(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-1-(2-(4-fluorophenylamino)phenyl)ethanone oxime(1246849-42-2)
• EPA Substance Registry System: (E)-1-(2-(4-fluorophenylamino)phenyl)ethanone oxime(1246849-42-2)

Safety Data

• Hazardous Substances Data: 1246849-42-2(Hazardous Substances Data)

Upstream product

• 1246849-59-1 1-(2-((4-fluorophenyl)amino)phenyl)ethanone 

Downstream Products

• 1213236-32-8 1-(4-fluorophenyl)-3-methyl-1H-indazole 
• 14207-43-3 1-(4-fluorophenyl)-2-methyl-1H-benzo[d]imidazole 

Relevant articles and documents

Synthesis of N-arylindazoles and benzimidazoles from a common intermediate

A variety of N-aryl-1H-indazoles and benzimidazoles were synthesized from common arylamino oximes in good to excellent yields. The product selectivity depends upon the base used in the reaction, as triethylamine promoted the formation of benzimidazoles, whereas 2-aminopyridine promoted the formation of N-arylindazoles. This method is valuable to the synthetic community because both indazoles and benzimidazoles are prevalent in pharmaceuticals.