1434474-99-3

Basic information

• Product Name: (1-(4-methoxyphenyl)-6-methyl-4,6-diphenyl-1,6-dihydropyridin-3-yl)(phenyl)methanone
• Synonyms: (1-(4-methoxyphenyl)-6-methyl-4,6-diphenyl-1,6-dihydropyridin-3-yl)(phenyl)methanone
• CAS NO: 1434474-99-3
• Molecular Weight: 457.572
• Mol File: 1434474-99-3.mol

Chemical Properties

• CAS DataBase Reference: (1-(4-methoxyphenyl)-6-methyl-4,6-diphenyl-1,6-dihydropyridin-3-yl)(phenyl)methanone(CAS DataBase Reference)
• NIST Chemistry Reference: (1-(4-methoxyphenyl)-6-methyl-4,6-diphenyl-1,6-dihydropyridin-3-yl)(phenyl)methanone(1434474-99-3)
• EPA Substance Registry System: (1-(4-methoxyphenyl)-6-methyl-4,6-diphenyl-1,6-dihydropyridin-3-yl)(phenyl)methanone(1434474-99-3)

Safety Data

• Hazardous Substances Data: 1434474-99-3(Hazardous Substances Data)

Upstream product

• 5876-69-7 2,4-diphenylbut-3-yn-2-ol 
• 25174-15-6 (Z)-3-((4-methoxyphenyl)amino)-1-phenylprop-2-en-1-one 
• 15753-62-5 <2-(4-Methoxy-anilino)-vinyl>-phenyl-keton 

Relevant articles and documents

Efficient iron-catalyzed synthesis of polysubstituted 1,2-dihydropyridine derivatives

A simple ligand-free cyclization of propargylic alcohols with enaminones has been developed by using FeBr3 as catalyst. This reaction provides an easy and convenient method to synthesize polysubstituted 1,2-dihydropyridine derivatives.

Lewis acid-catalyzed cyclization of enaminones with propargylic alcohols: Regioselective synthesis of multisubstituted 1,2-dihydropyridines

A highly efficient BF3·Et2O-catalyzed cascade reaction of enaminones with propargylic alcohols under mild reaction conditions has been developed. This methodology offers regioselective access to multisubstituted 1,2-dihydropyridines in good to excellent yields.