105997-06-6

Upstream product

• 18600-52-7 2-(4-chlorophenyl)-4H-benzo[d][1,3]oxazin-4-one 
• 24192-81-2 2-(2-iodophenyl)-1H-benzo[d]imidazole 
• 6212-33-5 2-(4-Chlorophenyl)glycine 
• 13275-42-8 2-(2-bromophenyl)-benzimidazole 
• 104-88-1 4-chlorobenzaldehyde 
• 118-92-3 anthranilic acid 
• 122-01-0 4-chloro-benzoyl chloride 
• 200626-58-0 1-(4-chlorobenzoyl)-2-(2-nitrophenyl)-1H-benzimidazole 
• 2208-58-4 2-(2-nitrophenyl)-1H-benzimidazole 
• 313480-92-1 N-[2-(1H-benzimidazol-2-yl)phenyl]-4-chlorobenzamide 
• 244032-48-2 2-(4-chlorophenyl)-3-(2-aminophenyl)quinazolin-4(3H)-one 
• 95-54-5 1,2-diamino-benzene 
• 5805-39-0 2-(aminophenyl)benzimidazole 

Downstream Products

• 940968-03-6 C₂₆H₂₄BN₃O₂ 

Relevant academic research and scientific papers

A new compound and an organic electronic device using the same

The present invention provides a new compound and an organic electronic device using the same. The compound according to the present invention may serve as hole injection, hole transporting, electron injection and transporting, and light emitting materials and the like in an organic electronic device comprising an organic light emitting device, and the organic electronic device according to the present invention shows excellent properties in terms of efficiency, driving voltage and service life.

Copper-mediated aerobic oxidative synthesis of benzimidazo fused quinazolines via a multicomponent approach

The first copper mediated aerobic oxidative multi-component synthesis of benzimidazo[1,2-c]quinazolines has been developed from 2-(2-halophenyl)benzoimidazoles, aldehydes and sodium azide as a nitrogen source. This protocol involves the formation of three

General and efficient copper-catalyzed aerobic oxidative synthesis of N-fused heterocycles using amino acids as the nitrogen source

A general and efficient copper-catalyzed aerobic oxidative method for the synthesis of N-fused heterocycles has been developed by using readily available α-amino acids as the nitrogen source. The reactions underwent N-arylation, aerobic oxidative dehydrogenation, intramolecular cyclization and dissociation of formic acid. This method should provide a general and practical strategy for the construction of N-fused heterocycles.

Solvent-Free Synthesis of 6-Arylbenzimidazo[1,2-c]quinazolines under Microwave Irradiation

The syntheses of 2-(2-nitrophenyl)-1-benzoyl-1H-benzimidazole derivatives 5-9 and their reduction to the corresponding 2-benzimidazoylbenzamides 10-13 are described. Compounds 10-13 were cleanly and efficiently converted to the corresponding 6-arylbenzimi

Synthesis of benzimidazo[1,2-c]quinazolines as possible bronchodilators

Synthesis of some 6-aryl-benzimidazo[1,2-c]quinazolines 4 have been critically investigated. The first method, based on the condensation of substituted-1,3-benzoxazin-4-(3H)-one 2 with o-phenylenediamine followed by cyclization of the resulting 2-aryl-3-(