He, Xiaohui team published research on Polymer in 2021 | 1739-84-0

Electric Literature of 1739-84-0, 1,2-Dimethylimidazole is used in the synthesis of 1,2-dimethyl-3-n-butylimidazoliumchloride and 1,2-dimethyl-3-n-propylimidazolium chloride. It also can be used in the synthesis of 1-(2-methoxyethyl)-2,3-dimethylimidazolium chloride and hexafluorophosphate salts.
1,2-Dimethylimidazole is a heterocyclic compound that contains nitrogen and carbon. It can be produced by the reaction between glyoxal and fatty acid in the presence of a base. 1,2-Dimethylimidazole has been shown to have biological properties such as an antioxidant effect. It is also used as a chemical intermediate for production of other chemicals such as 2-methylimidazole and 3-methylimidazole. 1,2-Dimethylimidazole has been shown to react with metal carbonyls to produce methylimines, which are useful intermediates in organic synthesis. The reaction mechanism involves hydrogen bonding and steric interactions between the imidazole ring and the metal carbonyl reactant., 1739-84-0.

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. 1739-84-0, formula is C5H8N2, Name is 1,2-Dimethyl-1H-imidazole. Their solubility in alcohol is lower than that in water and decreases with increasing molecular weight of the alcohols . Electric Literature of 1739-84-0.

He, Xiaohui;Zou, Jianhua;Guo, Yan;Wang, Kai;Wu, Bin;Wen, Yufei;Zang, Xiujing;Chen, Defu research published 《 Synthesis of halogenated benzonorbornadiene monomer and preparation of self-crosslinking bisimidazole cationic functionalized benzonorbornadiene triblock copolymer anion exchange membrane》, the research content is summarized as follows. In this paper, a series of anion exchange membranes of bisimidazolium functionalized triblock copolymers were synthesized by ring-opening metathesis polymerization of alkyl bromide functionalized benzonorbornadiene derivatives, 1,2-di-Me imidazole and epoxy functionalized norbornene under the action of Grubbs 2nd catalyst. The designed decomposition temperature of the triblock copolymer anion exchange membrane (AEM) exceeded 320 °C, which was much higher than the actual working temperature of anion exchange membrane fuel cell. TEM and AFM characterization proved that the AEM had formed an obvious microphase separation structure. The OH- conductivity of AEM-40 at 80 °C was as high as 56.09 mS cm-1. The single cell performance of the prepared AEM was tested at 60 °C, and we found that AEM-40 reached the highest power d. of 189.1 mW cm-2 at 352.1 mA cm-2.

Electric Literature of 1739-84-0, 1,2-Dimethylimidazole is used in the synthesis of 1,2-dimethyl-3-n-butylimidazoliumchloride and 1,2-dimethyl-3-n-propylimidazolium chloride. It also can be used in the synthesis of 1-(2-methoxyethyl)-2,3-dimethylimidazolium chloride and hexafluorophosphate salts.
1,2-Dimethylimidazole is a heterocyclic compound that contains nitrogen and carbon. It can be produced by the reaction between glyoxal and fatty acid in the presence of a base. 1,2-Dimethylimidazole has been shown to have biological properties such as an antioxidant effect. It is also used as a chemical intermediate for production of other chemicals such as 2-methylimidazole and 3-methylimidazole. 1,2-Dimethylimidazole has been shown to react with metal carbonyls to produce methylimines, which are useful intermediates in organic synthesis. The reaction mechanism involves hydrogen bonding and steric interactions between the imidazole ring and the metal carbonyl reactant., 1739-84-0.

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem