384824-41-3

Upstream product

• 384824-43-5 C₈H₈O₃*C₁₈H₁₇F₆N 
• 384824-40-2 C₁₈H₁₇F₆N*ClH 
• 30071-93-3 3,5-bis(trifluoromethyl)phenyl methyl ketone 
• 2627-86-3 (S)-1-phenyl-ethylamine 
• 672906-98-8 [1-(3,5-Bis-trifluoromethyl-phenyl)-eth-(E)-ylidene]-((S)-1-phenyl-ethyl)-amine 

Downstream Products

• 127733-40-8 (S)-α-(3,5-bis(trifluoromethyl)phenyl)ethylamine 
• 672907-00-5 C₄H₄O₄*C₁₈H₁₇F₆N 
• 127733-47-5 (R)-α-(3,5-bis(trifluoromethyl)phenyl)ethylamine 
• 384824-43-5 C₈H₈O₃*C₁₈H₁₇F₆N 
• 384824-40-2 C₁₈H₁₇F₆N*ClH 
• 672907-04-9 C₂₀H₂₁F₆N 
• 511256-36-3 (S)-1-(3,5-bis(trifluoromethyl)phenyl)-N-methylethanamine 
• 511256-31-8 [(S)-1-(3,5-Bis-trifluoromethyl-phenyl)-ethyl]-methyl-((S)-1-phenyl-ethyl)-amine 

Relevant academic research and scientific papers

Process for producing optically active 1-(fluoro- or trifluoromethyl-substituted phenyl) ethylamine and process for purifying same

An optically active 1-(fluoro- or trifluoromethyl-substituted phenyl)ethylamine is produced with high optical purity and in an industrially simple and efficient manner by asymmetrically reducing an optically active imine, obtained by dehydration and conde

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

Highly regioselective hydrogenolysis of bis(α-methylbenzyl)amine derivatives affected by the trifluoromethyl substituent on the aromatic ring

(Matrix presented) The highly regioselective hydrogenolysis of bis(α-methylbenzyl)amine derivatives proceeded with influence not from the electronic effect but from the steric effect of the trifluoromethyl substituent on the aromatic ring to provide a practical asymmetric synthesis of trifluoromethyl-substituted α-phenylethylamines.