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 . Computed Properties of 1739-84-0.
Schafer, Fabian;Neumann, Beate;Stammler, Hans-Georg;Mitzel, Norbert W. research published 《 Hexadentate Poly-Lewis Acids Based on 1,3,5-Trisilacyclohexane》, the research content is summarized as follows. We report the preparation of hexadentate poly-Lewis acids (PLA) based on 1,3,5-trisilacyclohexane backbones bearing two alkynyl groups attached to each of the silicon atoms. A rigid hexadentate PLA bearing six Lewis-acidic catecholatoboryl-substituents was prepared by a tin-boron exchange reaction. Its structure, determined by X-ray diffraction, is the first of a Lewis-acid-functionalised donor-free trisilacyclohexane. Flexible hexadentate PLA were prepared by hydroboration or hydrosilylation of hexavinyltrisilacyclohexane, resulting in PLA with six 9-BBN, SiCl3, SiCl2Me or SiClMe2 groups. The Lewis-acidity of the last one was increased by conversion with silver triflate, resulting in a PLA with six highly acidic silyl triflate groups attached to the 1,3,5-trisilacyclohexane unit as TfOSiMe2-C2H4– groups. Host-guest experiments of the above PLA demonstrated the suitability of the flexible representatives for complexation of neutral Lewis-based guest mols. under formation of 1 : 6 adducts (host: guest).
Computed Properties 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