62197-91-5

Basic information

• Product Name: N-(1-phenylethyl)-2,2,2-trifluoro-1-phenylethan-1-imine
• Synonyms: N-(1-phenylethyl)-2,2,2-trifluoro-1-phenylethan-1-imine
• CAS NO: 62197-91-5
• Molecular Weight: 277.289
• Mol File: 62197-91-5.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: N-(1-phenylethyl)-2,2,2-trifluoro-1-phenylethan-1-imine(CAS DataBase Reference)
• NIST Chemistry Reference: N-(1-phenylethyl)-2,2,2-trifluoro-1-phenylethan-1-imine(62197-91-5)
• EPA Substance Registry System: N-(1-phenylethyl)-2,2,2-trifluoro-1-phenylethan-1-imine(62197-91-5)

Safety Data

• Hazardous Substances Data: 62197-91-5(Hazardous Substances Data)

Upstream product

• 434-45-7 2,2,2-Trifluoroacetophenone 
• 2627-86-3 (S)-1-phenyl-ethylamine 

Downstream Products

• 62197-92-6 (αS)-α-(trifluoromethyl)-N-[(S)-1-phenylethyl]benzenemethanamine 
• 128444-37-1 ((1R,4S)-7,7-Dimethyl-2-oxo-bicyclo[2.2.1]hept-1-yl)-methanesulfonic acid; compound with 2,2,2-trifluoro-1-phenyl-ethylamine 
• 13652-09-0 (RS)-1-phenyl-2,2,2-trifluoroethylamine hydrochloride 
• 128404-36-4 [1-Phenyl-eth-(E)-ylidene]-(2,2,2-trifluoro-1-phenyl-ethyl)-amine 

Relevant articles and documents

Stereoselective metal-free catalytic synthesis of chiral trifluoromethyl aryl and alkyl amines

The enantioselective organocatalytic reduction of trifluoromethyl aryl and alkyl ketoimines afforded the corresponding fluorinated amines with high chemical and stereochemical efficiency. The Lewis base catalyzed reaction with trichlorosilane led to chiral products with a trifluoromethyl group directly linked to the newly generated stereocenter typically in >90% yield and up to 98% e.e.