177589-02-5

Basic information

• Product Name: [5-(4-Chloro-phenyl)-[1,3,4]oxadiazol-2-yl]-[2,2,2-trichloro-1-(4-chloro-phenyl)-ethyl]-amine
• CAS NO: 177589-02-5
• Molecular Weight: 437.54
• Mol File: 177589-02-5.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: [5-(4-Chloro-phenyl)-[1,3,4]oxadiazol-2-yl]-[2,2,2-trichloro-1-(4-chloro-phenyl)-ethyl]-amine(CAS DataBase Reference)
• NIST Chemistry Reference: [5-(4-Chloro-phenyl)-[1,3,4]oxadiazol-2-yl]-[2,2,2-trichloro-1-(4-chloro-phenyl)-ethyl]-amine(177589-02-5)
• EPA Substance Registry System: [5-(4-Chloro-phenyl)-[1,3,4]oxadiazol-2-yl]-[2,2,2-trichloro-1-(4-chloro-phenyl)-ethyl]-amine(177589-02-5)

Safety Data

• Hazardous Substances Data: 177589-02-5(Hazardous Substances Data)

Upstream product

• 76-03-9 trichloroacetic acid 
• 5315-86-6 4-chlorobenzaldehyde semicarbazone 
• 33621-61-3 2-amino-5-(4-chlorophenyl)-1,3,4-oxadiazole 
• 91872-90-1 N-(4-chlorobenzylidene)-5-(4-chlorophenyl)-1,3,4-oxadiazol-2-amine 

Relevant articles and documents

A new route for the convenient synthesis of imidazo[2,1-b]-1,3,4-oxadiazoles and their fungitoxicity

5-Aryl-1-arylideneamino-1,3,4-oxadiazoles (4a-f) react with trichloroacetic acid with the evolution of carbon dioxide to furnish 5-aryl-2-[(1-aryl-2,2,2-trichloroethyl)amino]-1,3,4-oxadiazoles (6a-f), which undergo ring closure with primary arylamines to