65964-65-0

Basic information

• Product Name: 7-methyl-2,3-dibenzimidazo[1,2-α]pyridine
• Synonyms: 7-methyl-2,3-dibenzimidazo[1,2-α]pyridine
• CAS NO: 65964-65-0
• Molecular Weight: 284.36
• Mol File: 65964-65-0.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 7-methyl-2,3-dibenzimidazo[1,2-α]pyridine(CAS DataBase Reference)
• NIST Chemistry Reference: 7-methyl-2,3-dibenzimidazo[1,2-α]pyridine(65964-65-0)
• EPA Substance Registry System: 7-methyl-2,3-dibenzimidazo[1,2-α]pyridine(65964-65-0)

Safety Data

• Hazardous Substances Data: 65964-65-0(Hazardous Substances Data)

Upstream product

• 695-34-1 2-Amino-4-methylpyridine 
• 2216-94-6 phenylpropynoic acid ethyl ester 
• 882187-78-2 7-methyl-3-phenylimidazo[1,2-α]pyridine 
• 108-95-2 phenol 
• 59-88-1 phenylhydrazine hydrochloride 
• 885-91-6 2-phenyl-7-methylimidazo[1,2-a]pyridine 
• 70-11-1 α-bromoacetophenone 
• 108-86-1 bromobenzene 
• 451-40-1 phenyl benzyl ketone 

Relevant articles and documents

Method for synthesizing benzimidazole compound and agricultural biological activity thereof

The invention provides a method for synthesizing a benzimidazole compound and the agricultural biological activity thereof, and belongs to the field of organic synthesis. The method has the advantagesof low raw material cost, no need of heating a reaction

Transition-metal-free C-C bond cleavage and formation: Efficient synthesis of 2,3-diarylimidazo[1,2-α]pyridines from 2-aminopyridines and alkynoates

A highly efficient transition-metal-free cyclization reaction for the synthesis of 2,3-diarylimidazo[1,2-α]pyridines is described. A variety of substituted 2-aminopyridines and alkynoates are compatible under the standard conditions. This protocol is marked by the cleavage of a C-C bond and the formation of a new Csp2-Csp2 bond under transition-metal-free conditions.

Copper-catalyzed synthesis of imidazo[1,2-a]pyridines through tandem imine formation-oxidative cyclization under ambient air: One-step synthesis of zolimidine on a gram-scale

A new copper-catalyzed oxidative cyclization via C-H amination between 2-aminopyridines and methyl aryl/heteroaryl ketones has been developed under ambient air. Imidazo[1,2-a]pyridines containing a wide range of functional groups have been synthesized from basic and easily available starting materials. This simple, one-pot reaction protocol is applicable for the direct preparation of zolimidine (a marketed antiulcer drug) on a large scale. Copyright