Electronic structure-activity relationships for propenone derivatives. II. 2-Cinnamoylbenzimidazoles and 2-(β-benzoylvinyl)-1-methylbenzimidazoles was written by Oganesyan, E. T.;Pogrebnyak, A. V.;Shiryaev, I. N.;Saraf, A. S.;Ivashev, M. N.. And the article was included in Khimiko-Farmatsevticheskii Zhurnal in 1995.Application In Synthesis of 1-Methyl-1H-benzo[d]imidazole-2-carbaldehyde This article mentions the following:
Synthesis of the title propenone derivatives as well as their sedative and antiallergic activities as functions of their electronic structure are described. In the experiment, the researchers used many compounds, for example, 1-Methyl-1H-benzo[d]imidazole-2-carbaldehyde (cas: 3012-80-4Application In Synthesis of 1-Methyl-1H-benzo[d]imidazole-2-carbaldehyde).
1-Methyl-1H-benzo[d]imidazole-2-carbaldehyde (cas: 3012-80-4) belongs to imidazole derivatives. Imidazole derivatives generally have good solubility in protic solvents. Simple imidazole derivatives, such as 1H-imidazole, 2-methyl-1H-imidazole, and 1,2-dimethylimidazole, have very high solubility in water. Imidazole derivatives have antibacterial, antifungal and anticancer functionality. It interacts with DNA and also binds to protein and stops cell division.Application In Synthesis of 1-Methyl-1H-benzo[d]imidazole-2-carbaldehyde
Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem