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. COA of Formula: C5H8N2.
Niizeki, Takeru;Hoshina, Taka-Aki;Takahashi, Tomoki research published 《 Characterizations of thermo-responsive alkyl imidazolium perchlorates for forward osmosis membrane process》, the research content is summarized as follows. The forward osmosis (FO) process uses a spontaneous water permeation phenomenon driven by an osmotic pressure difference between a feed solution (FS) and a draw solution (DS) through a semipermeable membrane. Hence, it is assumed that seawater desalination and feed solution concentration using FO processes can be conducted at low energy and cost. It is crucial to develop an optimal DS for the FO process before it can be put into practical use. The DS must have the following characteristics: (1) Develops higher osmotic pressure than FS, (2) Easy to regenerate and recover, (3) Low leakage, and (4) Low viscosity. Particularly, we propose low-grade waste heat to reduce energy consumption during DS regeneration and chose a temperature phase transition type DS that separates into water and solute components based on thermal response. In this study, we synthesized six alkyl imidazolium type ionic liquids (ILs) having perchlorate anion ([ClO4]), phase transition characteristics, and osmotic pressure, and the consequent FO performance was examined The synthesized ILs, 1-ethyl-3-propylimidazolium perchlorate [Im (2.0.3)] [ClO4] and 1,2-dimethyl-3-propylimidazolium perchlorate [Im(1.1.3)][ClO4], showed an upper critical solution temperature type phase transition in the temperature range of 25 ° to 50 °. The FO test confirms that pure water can be derived from saltwater using the osmotic pressure of DS. In comparison to other synthesized ILs, [Im (1.1.3)] [ClO4] showed higher performance in phase diagrams and osmotic pressure.
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., COA of Formula: C5H8N2
Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem