The three-dimensional configuration of the ester heterocycle is basically the same as that of the carbocycle. Compound: Pyridine-3,5-dicarbonitrile(SMILESS: N#CC1=CC(C#N)=CN=C1,cas:1195-58-0) is researched.Reference of Ethyl oxazole-5-carboxylate. The article 《Alkylation of pyridine-3,5-dicarboxamide and pyridine-3,5-dicarbonitriles by radical substitution》 in relation to this compound, is published in Journal of Heterocyclic Chemistry. Let’s take a look at the latest research on this compound (cas:1195-58-0).
Structural modification of NAD(P) model compounds, N,N,N’,N’-tetramethylpyridine-3,5-dicarboxamide (1), pyridine-3,5-dicarbonitrile (2), and 4-methylpyridine-3,5-dicarbonitrile (3), have been explored by the reaction with alkyl radicals such as the 1-adamantyl, tert-Bu, and iso-Pr radicals. The alkyl substitutions of compounds 1, 2, and 3 with the 1-adamantyl and the tert-Bu radical gave both 2-mono and 2,6-disubstitution products, whereas the reaction of compound 2 with the iso-Pr radical gave 2-mono- I, 2,4-di-, 2,6-di-, and 2,4,6-trisubstitution products.
In some applications, this compound(1195-58-0)Electric Literature of C7H3N3 is unique.If you want to know more details about this compound, you can contact with the author or consult more relevant literature.
Reference:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts