1286729-10-9

Basic information

• Product Name: 4-(2',4'-dichlorophenyl)-2,6-diphenylpyridine
• Synonyms: 4-(2',4'-dichlorophenyl)-2,6-diphenylpyridine
• CAS NO: 1286729-10-9
• Molecular Weight: 376.285
• Mol File: 1286729-10-9.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 4-(2',4'-dichlorophenyl)-2,6-diphenylpyridine(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(2',4'-dichlorophenyl)-2,6-diphenylpyridine(1286729-10-9)
• EPA Substance Registry System: 4-(2',4'-dichlorophenyl)-2,6-diphenylpyridine(1286729-10-9)

Safety Data

• Hazardous Substances Data: 1286729-10-9(Hazardous Substances Data)

Upstream product

• 95-73-8 2,4-dichlorotoluene 
• 19433-17-1 acetophenone O-acetyloxime 
• 874-42-0 2,4-dichlorobenzaldeyhde 
• 98-86-2 acetophenone 
• 613-91-2 acetophenone oxime 

Relevant articles and documents

One-Pot Synthesis of Benzene and Pyridine Derivatives via Copper-Catalyzed Coupling Reactions

A highly efficient one-pot synthesis of polysubstituted pyridine has been achieved through copper-catalyzed oxidative sp3 C?H coupling of acetophenones with toluene derivatives. Besides, the polysubstituted benzene was obtained through copper-catalyzed coupling of acetophenones. Both of the reactions exhibited a good functional group tolerance to produce a 2,4,6-triphenylpyridine or 1,3,5-triarylbenzene in high yields. Compared with previous methods, these transformations allow a highly flexible and efficient preparation of substituted pyridines and benzenes. (Figure presented.).

Synthesis of Polyfunctional Pyridines via Copper-Catalyzed Oxidative Coupling Reactions

An efficient and concise approach for the synthesis of polysubstituted pyridines has been achieved through copper-catalyzed oxidative sp3 C-H coupling of oxime acetates with toluene derivatives. Besides, benzylamine and p-toluenesulfonylhydrazo

Copper-Catalyzed coupling of oxime acetates with aldehydes: A new strategy for synthesis of pyridines

Copper-catalyzed coupling of oxime acetates with aldehydes offers a new strategy for the synthesis of highly substituted pyridines. This novel method tolerates a wide range of functionality and allows for rapid elaboration of the oxime acetates into a variety of substituted pyridines.