Ring-opening of N-tosyl aziridines with hydroxyl compounds catalyzed by acidic ionic liquid was written by Li, Yuling;Gu, Dagong;Xu, Xiaoping;Ji, Shunjun. And the article was included in Chinese Journal of Chemistry in 2009.Related Products of 478935-29-4 The following contents are mentioned in the article:
The ring-opening of two types of N-tosyl aziridines with hydroxyl compounds was studied. The aziridines reacted smoothly with alcs. in the presence of functional ionic liquid [hmim]HSO4 to afford the corresponding β-amino ethers in moderate to good yields with high regioselectivity. The recyclable property of [hmim]HSO4 was demonstrated in the process. This study involved multiple reactions and reactants, such as 1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate (cas: 478935-29-4Related Products of 478935-29-4).
1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate (cas: 478935-29-4) belongs to imidazole derivatives. Among the different heterocyclic compounds, imidazole is better known due to its broad range of chemical and biological properties. Imidazole has become an important synthon in the development of new drugs. Imidazole is incorporated into many important biological compounds. The most pervasive is the amino acid histidine, which has an imidazole side-chain. Histidine is present in many proteins and enzymes, e.g. by binding metal cofactors, as seen in hemoglobin.Related Products of 478935-29-4
Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem