Photoreactions of aromatic compounds. XXXVI. Nucleophilic photosubstitution reactions of some derivatives of imidazole and pyrazole was written by Oldenhof, C.;Cornelisse, J.. And the article was included in Recueil des Travaux Chimiques des Pays-Bas in 1978.Recommanded Product: 3034-41-1 This article mentions the following:
Nucleophilic photosubstitution of nitro derivatives of 1-methylimidazole and 1-methylpyrazole strongly depends on the position of the nitro group. In the imidazole series the 5-nitro compound is the most reactive isomer; photochem. replacement of the nitro group by cyano or methoxy proceeds in good yield. On the nitro-substituted 1-methylpyrazoles, the 3-nitro derivative is the most reactive isomer; photocyanation yields equal amounts of 1-methyl-3-nitro-4-cyanopyrazole and 1-methyl-3-nitrosopyrazole. Some of the reactions proceed by normal bimol. aromatic photosubstitution; others bear resemblance to the photoreactions of methoxybenzenes and -naphthalenes in which a cation radical is intermediate. In the experiment, the researchers used many compounds, for example, 1-Methyl-4-nitroimidazole (cas: 3034-41-1Recommanded Product: 3034-41-1).
1-Methyl-4-nitroimidazole (cas: 3034-41-1) belongs to imidazole derivatives. Imidazole is a heterocyclic compound with a five-membered planar ring. It is amphoteric and highly polar. Imidazole derivatives have antibacterial, antifungal and anticancer functionality. It interacts with DNA and also binds to protein and stops cell division.Recommanded Product: 3034-41-1
Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem