Wang, Jian team published research in Journal of Molecular Liquids in 2022 | 1739-84-0

Product Details of C5H8N2, 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 Biochem/physiol Actions: Imidazole derivatives have antibacterial, antifungal and anticancer functionality. It interacts with DNA and also binds to protein and stops cell division. 1739-84-0, formula is C5H8N2, Name is 1,2-Dimethyl-1H-imidazole. It also acts as a microtubule destabilizing agents and inhibits topoisomerase and Cytochrome P450 Family 26 Subfamily A Member 1 (CYP26A1) enzymes. Product Details of C5H8N2.

Wang, Jian;Li, Yuao;Chen, Xiguang;Wei, Ning;Tong, Jing research published 《 Excess properties and activation properties for viscous flow of amino acid ionic liquids with H2O binary mixtures》, the research content is summarized as follows. Amino acid ionic liquids (ILs) 1-butyl-2,3-dimethylimidazolium glycine ([C4Dmim][Gly]), 1-butyl-2,3-dimethylimidazolium alanine ([C4Dmim][Ala]) and 1-butyl-2,3-dimethylimidazolium threonine ([C4Dmim][Thr]) were prepared Over the temperature from (288.15-318.15) K, the d., surface tension and viscosity for binary system mixtures of ILs with H2O were measured, and excess thermodn. properties and activation properties for viscous flow of these binary system mixtures were systematically studied. Secondly, the variation trend between excess molar volume (VE)/excess molar surface Gibbs energy (gEs) and mole fraction for ILs + H2O binary system mixtures was investigated. With the increase of mole fraction, the VE and gEs values of binary system mixtures increased firstly and then decreased, and they were pos. value, which may be due to the weak chem. interaction between ILs and H2O in the mixture Furthermore, according to the thermodn. formula, the Gibbs energy of activation for viscous flow of the relative viscosity (ΔG≠r), activation entropy (ΔS≠r) and activation enthalpy (ΔH≠r) were calculated Over the entire concentration range, the ΔG≠r values for binary system mixtures of ILs with H2O were neg. value, and the result was in good agreement with relative viscosity (ηr).

Product Details of C5H8N2, 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