1001915-83-8

Basic information

• Product Name: 1-phenyl-2-tridecyl-1H-benzoimidazole
• Synonyms: 1-phenyl-2-tridecyl-1H-benzoimidazole
• CAS NO: 1001915-83-8
• Molecular Weight: 376.585
• Mol File: 1001915-83-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1-phenyl-2-tridecyl-1H-benzoimidazole(CAS DataBase Reference)
• NIST Chemistry Reference: 1-phenyl-2-tridecyl-1H-benzoimidazole(1001915-83-8)
• EPA Substance Registry System: 1-phenyl-2-tridecyl-1H-benzoimidazole(1001915-83-8)

Safety Data

• Hazardous Substances Data: 1001915-83-8(Hazardous Substances Data)

Upstream product

• 609-73-4 o-nitroiodobenzene 
• 622-56-0 myristanilide 

Relevant articles and documents

A direct, regioselective palladium-catalyzed synthesis of N-substituted benzimidazoles and imidazopyridines

Unsymmetric, N-substituted benzimidazoles and imidazopyridines can be prepared directly from 2-halonitroarenes and amides through Pd(TFA) 2/(R)-BINAP-catalyzed cross-coupling and subsequent reductive aminocyclization. This sequence can be conducted by a one-pot procedure. The method is versatile and allows the straightforward, regioselective preparation of these important nitrogen heterocycles. Unsymmetrical, N-substituted benzimidazoles can be prepared directly from 2-halonitroarenes and amides through Pd(TFA)2/(R)-BINAP-catalyzed cross-coupling and subsequent reductive aminocyclization.This sequence can be conducted by a one-pot procedure. The method is versatile and allows the straightforward, regioselective preparation of these important nitrogen heterocycles. Copyright

A REGIOSELECTIVE COPPER CATALYZED SYNTHESIS OF BENZIMIDAZOLES AND AZABENZIMIDAZOLES

The present invention relates to a process for the regioselective synthesis of compounds of the formula (I), wherein R0; R1; R2; R3; R4; R5; A1; A2; A3; A4; Q and J have the meanings indicated in the claims. The present invention provides a direct copper catalyzed regioselective process to a wide variety of unsymmetrical, multifunctional N/-substituted benzimidazoles or azabenzimidazoles of formula I starting from 2-halo-nitroarenes and N/-substituted amides. The process is useful for the production of pharmaceuticals, diagnostic agents, liquid crystals, polymers, herbicides, fungicidals, nematicidals, parasiticides, insecticides, acaricides and arthropodicides.