511256-29-4

Basic information

• Product Name: [(R)-1-(3,5-Bis-trifluoromethyl-phenyl)-ethyl]-((S)-1-phenyl-ethyl)-amine
• Synonyms: [(R)-1-(3,5-Bis-trifluoromethyl-phenyl)-ethyl]-((S)-1-phenyl-ethyl)-amine
• CAS NO: 511256-29-4
• Molecular Weight: 361.33
• Mol File: 511256-29-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: [(R)-1-(3,5-Bis-trifluoromethyl-phenyl)-ethyl]-((S)-1-phenyl-ethyl)-amine(CAS DataBase Reference)
• NIST Chemistry Reference: [(R)-1-(3,5-Bis-trifluoromethyl-phenyl)-ethyl]-((S)-1-phenyl-ethyl)-amine(511256-29-4)
• EPA Substance Registry System: [(R)-1-(3,5-Bis-trifluoromethyl-phenyl)-ethyl]-((S)-1-phenyl-ethyl)-amine(511256-29-4)

Safety Data

• Hazardous Substances Data: 511256-29-4(Hazardous Substances Data)

Upstream product

• 672906-98-8 [1-(3,5-Bis-trifluoromethyl-phenyl)-eth-(E)-ylidene]-((S)-1-phenyl-ethyl)-amine 
• 384824-40-2 C₁₈H₁₇F₆N*ClH 
• 384824-43-5 C₈H₈O₃*C₁₈H₁₇F₆N 
• 672907-00-5 C₄H₄O₄*C₁₈H₁₇F₆N 
• 30071-93-3 3,5-bis(trifluoromethyl)phenyl methyl ketone 
• 2627-86-3 (S)-1-phenyl-ethylamine 

Downstream Products

• 127733-47-5 (R)-α-(3,5-bis(trifluoromethyl)phenyl)ethylamine 
• 384824-43-5 C₈H₈O₃*C₁₈H₁₇F₆N 
• 127733-40-8 (S)-α-(3,5-bis(trifluoromethyl)phenyl)ethylamine 
• 672907-00-5 C₄H₄O₄*C₁₈H₁₇F₆N 
• 384824-40-2 C₁₈H₁₇F₆N*ClH 
• 672907-02-7 C₁₉H₁₉F₆N 

Relevant articles and documents

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

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.