Recommanded Product: 62567-44-6On May 21, 1998 ,《Vicarious nucleophilic substitution of pyridazinium N-dicyanomethylides》 appeared in Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry. The author of the article were Itoh, Takashi; Matsuya, Yuji; Nagata, Kazuhiro; Miyazaki, Michiko; Tsutsumi, Nozomi; Ohsawa, Akio. The article conveys some information:
Pyridazines have been allowed to react with tetracyanoethylene oxide to give pyridazinium N-dicyanomethylides, which are subjected to vicarious nucleophilic substitution to afford the corresponding 4-substituted derivatives in moderate to good yields. The dicyanomethylene group is readily eliminated by a radical reaction, and 4-substituted pyridazines are obtained. The results came from multiple reactions, including the reaction of 3-Ethoxypyridazine(cas: 62567-44-6Recommanded Product: 62567-44-6)
3-Ethoxypyridazine(cas: 62567-44-6) belongs to pyridazine derivatives.The pyridazine derivatives are mostly present in biologically active compounds and are also present with different pharmacophores. Pyridazines are also important because of their utility in synthetic organic chemistry and in physical organic chemistry.There are reports available for the synthesis of pyridazine and their derivatives by using 2-oxoaldehyes.Recommanded Product: 62567-44-6
Referemce:
Pyridazine – Wikipedia,
Pyridazine | C4H4N2 – PubChem