122078-14-2

Basic information

• Product Name: [1-(2,6-Dimethoxy-phenyl)-eth-(E)-ylidene]-((S)-1-phenyl-ethyl)-amine
• CAS NO: 122078-14-2
• Molecular Weight: 283.37
• Mol File: 122078-14-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: [1-(2,6-Dimethoxy-phenyl)-eth-(E)-ylidene]-((S)-1-phenyl-ethyl)-amine(CAS DataBase Reference)
• NIST Chemistry Reference: [1-(2,6-Dimethoxy-phenyl)-eth-(E)-ylidene]-((S)-1-phenyl-ethyl)-amine(122078-14-2)
• EPA Substance Registry System: [1-(2,6-Dimethoxy-phenyl)-eth-(E)-ylidene]-((S)-1-phenyl-ethyl)-amine(122078-14-2)

Safety Data

• Hazardous Substances Data: 122078-14-2(Hazardous Substances Data)

Upstream product

• 2040-04-2 2,6-dimethoxyacetophenone 
• 2627-86-3 (S)-1-phenyl-ethylamine 

Downstream Products

• 122078-26-6 (1S,1'S)-N-(1'-phenylethyl)-1-(2'',6''-dimethoxyphenyl)ethylamine hydrobromide 
• 122209-82-9 (S)-1-(2',6'-dimethoxyphenyl)ethylamine hydrobromide 

Relevant articles and documents

ENANTIOMERICALLY PURE OXYGENATED 1-PHENYLETHYLAMINES FROM SUBSTITUTED ACETOPHENONES: BY REDUCTIVE AMINATION AND REGIOSPECIFIC CLEAVAGE

An efficient method for the asymmetric synthesis of chiral, oxygenated 1-phenylethylamines (1) in essentially two steps is described.The substituted acetophenones 2 are reductively aminated with unsubstituted chiral 1-phenylethylamine ("PEA",3), via the c