1329710-08-8

Basic information

• Product Name: N-benzyl-3-(4-ethylphenyl)-N-methyl-1-phenylprop-2-yn-1-amine
• Synonyms: N-benzyl-3-(4-ethylphenyl)-N-methyl-1-phenylprop-2-yn-1-amine
• CAS NO: 1329710-08-8
• Molecular Weight: 339.48
• Mol File: 1329710-08-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: N-benzyl-3-(4-ethylphenyl)-N-methyl-1-phenylprop-2-yn-1-amine(CAS DataBase Reference)
• NIST Chemistry Reference: N-benzyl-3-(4-ethylphenyl)-N-methyl-1-phenylprop-2-yn-1-amine(1329710-08-8)
• EPA Substance Registry System: N-benzyl-3-(4-ethylphenyl)-N-methyl-1-phenylprop-2-yn-1-amine(1329710-08-8)

Safety Data

• Hazardous Substances Data: 1329710-08-8(Hazardous Substances Data)

Upstream product

• 98-86-2 acetophenone 
• 40307-11-7 1-ethyl-4-ethynylbenzene 
• 103-67-3 benzyl-methyl-amine 
• 611-73-4 Benzoylformic acid 

Relevant articles and documents

1D Fe3O4&at;CuSiO3 composites catalyzed decarboxylative A3-coupling for propargylamine synthesis

Highly active and stable magnetic copper catalysts were successfully achieved by magnetic induced St?ber method and subsequent hydrothermal reaction with copper ions in alkaline condition. The high content of Cu2+ as well as the unique structures of hierarchical copper silicate in the as-prepared catalysts endowed their outstanding catalytic performance. Efficient decarboxylative A3-coupling of α-keto acid, amine and alkyne was realized with the low Fe3O4&at;CuSiO3 loading. A range of propargylamines were produced in good to excellent yields under solvent-free condition. Moreover, the catalyst can be easily separated from the final organic product with an external magnet. Also, this kind of catalyst could be recycled up to six times while maintaining its activity.