Free-radical polymerization and copolymerization of acrylonitrile in ionic liquids was written by Vygodskii, Ya. S.;Mel’nik, O. A.;Lozinskaya, E. I.;Shaplov, A. S.. And the article was included in Vysokomolekulyarnye Soedineniya, Seriya A i Seriya B in 2005.Synthetic Route of C7H13ClN2 This article mentions the following:
The free-radical polymerization of acrylonitrile and its copolymerization with Me methacrylate in ionic liquids based on 1,3-dialkyl-substituted imidazole were studied. It was shown that, in contrast to the case of common mol. solvents, the polymerization and copolymerization in liquid organic salts give high-mol.-mass polyacrylonitrile and copolymers with high yields, with the former polymer showing a higher onset temperature of degradation In the experiment, the researchers used many compounds, for example, 1-Methyl-3-propylimidazolium Chloride (cas: 79917-89-8Synthetic Route of C7H13ClN2).
1-Methyl-3-propylimidazolium Chloride (cas: 79917-89-8) belongs to imidazole derivatives. Many natural products, especially alkaloids, contain the imidazole ring. These imidazoles share the 1,3-C3N2 ring but feature varied substituents. Imidazole derivatives have antibacterial, antifungal and anticancer functionality. It interacts with DNA and also binds to protein and stops cell division.Synthetic Route of C7H13ClN2
Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem