Zeng, Hui team published research in Polymer in 2021 | 1739-84-0

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., Recommanded Product: 1,2-Dimethyl-1H-imidazole

The solubility of imidazoles in ethers is lower than that in alcohols and decreases with increasing chain length of the ethers . 1739-84-0, formula is C5H8N2, Name is 1,2-Dimethyl-1H-imidazole. In contrast, the solubility of benzimidazoles in alcohols (C3–C6) is higher than in water and generally decreases with an increase of the alkyl chain length of the alcohols. Recommanded Product: 1,2-Dimethyl-1H-imidazole.

Zeng, Hui;Tang, Zhenghai;Duan, Yun;Wu, Siwu;Guo, Baochun research published 《 Recyclable crosslinked elastomer based on dynamic dithioacetals》, the research content is summarized as follows. Recent progress in introducing elegant dynamic covalent bonds into covalently crosslinked networks enabled the trade-offs between chem. crosslinking and recycling. Thus far, continuous efforts are made to exploit new dynamic chemistries to address the constrains of intricate preparation procedures and need of catalyst additives in creating dynamic covalent networks. In this work, we report an industrially feasible process to prepare catalyst-free malleable elastomers by engineering dithioacetals as the dynamic motifs into a com. diene rubber. Specifically, a dithioacetal-containing diacid (BTA) is synthesized and used as a novel crosslinker for epoxidized natural rubber (ENR), by which dynamic dithioacetals are introduced into the elastomeric networks. Small mol. model study shows that dithioacetal exchange can be conducted at elevated temperature without catalyst. In the BTA crosslinked ENR, the thermoactivated dithioacetal exchange reactions can alter its network topologies in an associative pathway and confer it with remarkable reprocessability. The mech. properties and relaxation rate of the networks can be readily manipulated by varying the dithioacetal concentration

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., Recommanded Product: 1,2-Dimethyl-1H-imidazole

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem