104828-83-3

Basic information

• Product Name: (1R,1'R)-N-(1'-phenylethyl)-1-(4''-methoxyphenyl)ethylamine
• Synonyms: (1R,1'R)-N-(1'-phenylethyl)-1-(4''-methoxyphenyl)ethylamine
• CAS NO: 104828-83-3
• Molecular Weight: 255.36
• Mol File: 104828-83-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (1R,1'R)-N-(1'-phenylethyl)-1-(4''-methoxyphenyl)ethylamine(CAS DataBase Reference)
• NIST Chemistry Reference: (1R,1'R)-N-(1'-phenylethyl)-1-(4''-methoxyphenyl)ethylamine(104828-83-3)
• EPA Substance Registry System: (1R,1'R)-N-(1'-phenylethyl)-1-(4''-methoxyphenyl)ethylamine(104828-83-3)

Safety Data

• Hazardous Substances Data: 104828-83-3(Hazardous Substances Data)

Upstream product

• 1163726-09-7 C₁₇H₁₉NO 
• 100-06-1 1-(4-methoxyphenyl)ethanone 
• 3886-69-9 (R)-1-phenyl-ethyl-amine 
• 104873-93-0 [1-(4-Methoxy-phenyl)-eth-(E)-ylidene]-((R)-1-phenyl-ethyl)-amine 

Downstream Products

• 6298-96-0 1(R)-(4-methoxyphenyl)-ethylamine 

Relevant articles and documents

A convenient, highly stereoselective, metal-free synthesis of chiral amines

A low cost, efficient, metal-free highly stereoselective reduction of ketimines to chiral amines was developed. Different imines bearing a very cheap and removable chiral auxiliary were reduced simply by trichlorosilane in the presence of N,N-dimethylformamide, often in quantitative yield and complete control of the absolute stereochemistry, to afford highly enantiomerically enriched amines. Georg Thieme Verlag Stuttgart.

NADH MODELS XXI. STEREOSELECTIVE REDUCTION OF CHIRAL IMINES WITH HANTZSCH ESTER

Imines derived from p-substituted acetophenones and (+) R-1-phenylethylamine are reduced by 3,5-diethoxycarbonyl-2,6-dimethyl-1,4-dihydro-pyridine (Hantzsch ester), in acetonitrile, in the presence of magnesium perchlorate, to diastereomeric mixtures of t