161170-64-5

Basic information

• Product Name: (S)-1-phenyl-N-((furan-2-yl)methyl)ethanamine
• Synonyms: (S)-1-phenyl-N-((furan-2-yl)methyl)ethanamine
• CAS NO: 161170-64-5
• Molecular Weight: 201.268
• Mol File: 161170-64-5.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: (S)-1-phenyl-N-((furan-2-yl)methyl)ethanamine(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-1-phenyl-N-((furan-2-yl)methyl)ethanamine(161170-64-5)
• EPA Substance Registry System: (S)-1-phenyl-N-((furan-2-yl)methyl)ethanamine(161170-64-5)

Safety Data

• Hazardous Substances Data: 161170-64-5(Hazardous Substances Data)

Upstream product

• 120408-88-0 (S)-N-2-furylmethylidene-1-phenylethylamine 
• 111187-95-2 [1-Furan-2-yl-meth-(E)-ylidene]-((S)-1-phenyl-ethyl)-amine 
• 98-01-1 furfural 
• 2627-86-3 (S)-1-phenyl-ethylamine 
• 617-89-0 furan-2-ylmethanamine 
• 98-86-2 acetophenone 

Downstream Products

• 918476-40-1 (S,S)-N,N'-bis-furan-2-ylmethyl N,N'-bis-(1-phenylethyl)-oxalamide 
• 477788-34-4 Ethenesulfonic acid furan-2-ylmethyl-((S)-1-phenyl-ethyl)-amide 

Relevant articles and documents

Asymmetric synthesis of methyl N-(1-phenylethyl)-3-aza-10-oxatricyclo[5.2.1.01,5]-4-oxo dec-8-en-6-carboxylate by an intramolecular Diels-Alder reaction

The title compound can be obtained with up to five asymmetric centres of known absolute configuration by a diastereoselective intramolecular Diels-Alder reaction between optically active N-substituted furfurylamines and maleic anhydride, in which the chir

One-pot solvent-free reductive amination with a solid ammonium carbamate salt from CO2 and amine

Many amines are liquid and their handling is inconvenient compared with the corresponding solids. We transformed a liquid (S)-(-)-1-phenylethylamine 1 to the corresponding neutral solid form 2 by reacting with carbon dioxide. We performed reductive aminat

Scope of the organocatalysed asymmetric reductive amination of ketones with trichlorosilane

A highly active organocatalyst has been shown to affect the asymmetric reductive amination of ketones producing both aromatic and aliphatic amines. At 1 mol% catalyst loading, a series of structurally diverse chiral amines were quickly and economically prepared with good enantioselectivity and generally useful yield. The efficient synthesis of the calcimimetic (+)-NPS R-568 (67%, 89% ee) demonstrated the synthetic applicability of this methodology.