672906-81-9

Basic information

• Product Name: [1-(4-Fluoro-phenyl)-eth-(E)-ylidene]-((S)-1-phenyl-ethyl)-amine
• Synonyms: [1-(4-Fluoro-phenyl)-eth-(E)-ylidene]-((S)-1-phenyl-ethyl)-amine
• CAS NO: 672906-81-9
• Molecular Weight: 241.308
• Mol File: 672906-81-9.mol

Chemical Properties

• CAS DataBase Reference: [1-(4-Fluoro-phenyl)-eth-(E)-ylidene]-((S)-1-phenyl-ethyl)-amine(CAS DataBase Reference)
• NIST Chemistry Reference: [1-(4-Fluoro-phenyl)-eth-(E)-ylidene]-((S)-1-phenyl-ethyl)-amine(672906-81-9)
• EPA Substance Registry System: [1-(4-Fluoro-phenyl)-eth-(E)-ylidene]-((S)-1-phenyl-ethyl)-amine(672906-81-9)

Safety Data

• Hazardous Substances Data: 672906-81-9(Hazardous Substances Data)

Upstream product

• 2627-86-3 (S)-1-phenyl-ethylamine 
• 403-42-9 1-(4-fluorophenyl)ethanone 

Downstream Products

• 444643-12-3 (R)-1-(4-fluorophenyl)-N-((S)-1-phenylethyl)ethan-1-amine 
• 66399-30-2 (S)-1-(4-Fluoro-phenyl)-ethylamine 
• 444643-11-2 (S)-1-phenyl-N-((S)-1-(4-(fluoro)phenyl)ethyl)ethan-1-amine 

Relevant articles and documents

Practical synthesis of optically active fluorine-substituted α-phenylethylamines by retardation of hydrogenolytic cleavage at benzylic position

High regioselectivity in hydrogenolysis of bis(α-methylbenzyl)amines having a fluorine atom on aromatic ring results from retardation of hydrogenolytic cleavage at benzylic position of fluorine-substituted aromatic ring.

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