137566-61-1

Basic information

• Product Name: [1-Methyl-2-[(E)-(R)-1-phenyl-ethylimino]-prop-(E)-ylidene]-((R)-1-phenyl-ethyl)-amine
• Synonyms: [1-Methyl-2-[(E)-(R)-1-phenyl-ethylimino]-prop-(E)-ylidene]-((R)-1-phenyl-ethyl)-amine
• CAS NO: 137566-61-1
• Molecular Weight: 292.424
• Mol File: 137566-61-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: [1-Methyl-2-[(E)-(R)-1-phenyl-ethylimino]-prop-(E)-ylidene]-((R)-1-phenyl-ethyl)-amine(CAS DataBase Reference)
• NIST Chemistry Reference: [1-Methyl-2-[(E)-(R)-1-phenyl-ethylimino]-prop-(E)-ylidene]-((R)-1-phenyl-ethyl)-amine(137566-61-1)
• EPA Substance Registry System: [1-Methyl-2-[(E)-(R)-1-phenyl-ethylimino]-prop-(E)-ylidene]-((R)-1-phenyl-ethyl)-amine(137566-61-1)

Safety Data

• Hazardous Substances Data: 137566-61-1(Hazardous Substances Data)

Upstream product

• 3886-69-9 (R)-1-phenyl-ethyl-amine 
• 431-03-8 dimethylglyoxal 

Downstream Products

• 36283-44-0 N-acetyl-1-phenylethylamine 
• 17329-20-3 (R)-(+)-α-methylbenzylisocyanide 
• 474888-41-0 5-methylene-1-[(1R)-1-phenylethyl]-4-[(1R)-1-phenylethylamine]-2,5-dihydro-1H-2-azolone 

Relevant articles and documents

A concise, asymmetric synthesis of tetramic acid derivatives

(graph presented) A simple, asymmetric synthesis of tetramic acid derivatives is described in this paper. The key step is a carbonyl transfer from carbonyldiimidazole (CDI) to α-diimines (I) to form N-alkyl-4-alkylamino-5-methylenepyrrol-2-ones (II). In t