112066-66-7

Basic information

• Product Name: (S)-N-methyl-3-(2-methoxyphenoxy)-3-phenyl-1-propanamine
• Synonyms: (S)-N-methyl-3-(2-methoxyphenoxy)-3-phenyl-1-propanamine
• CAS NO: 112066-66-7
• Molecular Weight: 271.359
• Mol File: 112066-66-7.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (S)-N-methyl-3-(2-methoxyphenoxy)-3-phenyl-1-propanamine(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-N-methyl-3-(2-methoxyphenoxy)-3-phenyl-1-propanamine(112066-66-7)
• EPA Substance Registry System: (S)-N-methyl-3-(2-methoxyphenoxy)-3-phenyl-1-propanamine(112066-66-7)

Safety Data

• Hazardous Substances Data: 112066-66-7(Hazardous Substances Data)

Upstream product

• 138750-31-9 (1R)-3-amino-1-phenyl-1-propanol 
• 191729-90-5 (S)-3-(2-Methoxy-phenoxy)-3-phenyl-propylamine 
• 191729-87-0 3-(2-methoxyphenoxy)-3-phenylpropanenitrile 
• 935-02-4 3-Phenyl-2-propynonitrile 
• 90-05-1 2-methoxy-phenol 
• 142037-19-2 Chloro-acetic acid (S)-3-chloro-1-phenyl-propyl ester 
• 100306-33-0 (1R)-3-chloro-1-phenylpropanol 
• 100306-34-1 3-chloro-1-phenylpropanol 
• 141987-54-4 1-Phenyl-3-chlor-propyl-monochloracetat 
• 18776-12-0 3-chloro-1-phenyl-propan-1-ol 
• 936-59-4 3-chloropropiophenone 
• 502697-62-3 (R)-(3-hydroxy-3-phenylpropyl)carbamic acid ethyl ester 
• 198561-42-1 (R)-3-acetyloxy-3-phenylpropanenitrile 
• 73627-97-1 3-hydroxy-3-phenylpropanenitrile 

Relevant articles and documents

Asymmetric Hydrogenation of β-Aryloxy/Alkoxy Cinnamic Nitriles and Esters

A highly efficient and enantioselective hydrogenation of β-aryloxy/alkoxy cinnamic nitriles and esters under mild conditions has been realized by using a rhodium catalyst with a chiral f-spiroPhos ligand. The method provides efficient access to the asymme

Chemoenzymatic synthesis of the non-tricyclic antidepressants Fluoxetine, Tomoxetine and Nisoxetine

3-Chloro-1-phenylpropan-1-ol and the corresponding butanoate, 3-chloro-1-phenyl-1-propyl butanoate, were kinetically resolved using lipase B from Candida antarctica catalysis by transesterification and hydrolysis respectively. The resulting chiral building blocks (S)- and (R)-3-chloro-1-phenylpropanol were converted into both enantiomers of the antidepressant drugs, Fluoxetine, Tomoxetine and Nisoxetine. The Royal Society of Chemistry 2000.