444643-05-4

Basic information

• Product Name: ((S)-1-Phenyl-ethyl)-[(R)-1-(4-trifluoromethyl-phenyl)-ethyl]-amine
• Synonyms: ((S)-1-Phenyl-ethyl)-[(R)-1-(4-trifluoromethyl-phenyl)-ethyl]-amine
• CAS NO: 444643-05-4
• Molecular Weight: 293.332
• Mol File: 444643-05-4.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: ((S)-1-Phenyl-ethyl)-[(R)-1-(4-trifluoromethyl-phenyl)-ethyl]-amine(CAS DataBase Reference)
• NIST Chemistry Reference: ((S)-1-Phenyl-ethyl)-[(R)-1-(4-trifluoromethyl-phenyl)-ethyl]-amine(444643-05-4)
• EPA Substance Registry System: ((S)-1-Phenyl-ethyl)-[(R)-1-(4-trifluoromethyl-phenyl)-ethyl]-amine(444643-05-4)

Safety Data

• Hazardous Substances Data: 444643-05-4(Hazardous Substances Data)

Upstream product

• 439084-89-6 C₆H₆O₃S*C₁₇H₁₈F₃N 
• 2627-86-3 (S)-1-phenyl-ethylamine 
• 709-63-7 1-(4-trifluoromethylphenyl)ethanone 
• 672906-91-1 (E)-N-(1-(S)-phenylethyl)ethan-1-(4-(trifluoromethyl)phenyl)-1-imine 

Downstream Products

• 84499-73-0 (S)-N-[α-ethyl-4-(trifluoromethyl)benzyl]amine 
• 578027-35-7 (R)-N-[α-ethyl-4-(trifluoromethyl)benzyl]amine 
• 439084-89-6 C₆H₆O₃S*C₁₇H₁₈F₃N 

Relevant articles and documents

Iron catalyzed diastereoselective hydrogenation of chiral imines

Cyclopentadienone-based iron complexes were used for the first time to successfully catalyze the diastereoselective hydrogenation of enantiopure imines. Chiral amines, including valuable biologically active products, were obtained often as enantiomericall

OPTICALLY ACTIVE 1-(FLUORO-,TRIFLUOROMETHYL-OR TRIFLUOROMETHOXY-SUBSTITUTED PHENYL)ALKYLAMINE N-MONOALKYL DERIVATIVES AND PROCESS FOR PRODUCING SAME

An optically active 1-(fluoro-, trifluoromethyl- or trifluoromethoxy-substituted phenyl)alkylamine N-monoalkyl derivative represented by the formula [4] is produced by a process including (a) reacting an optically active secondary amine, represented by th