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There is still a lot of research devoted to this compound(SMILES:N#CC1=CC(C#N)=CN=C1)Name: Pyridine-3,5-dicarbonitrile, and with the development of science, more effects of this compound(1195-58-0) can be discovered.

Name: Pyridine-3,5-dicarbonitrile. The protonation of heteroatoms in aromatic heterocycles can be divided into two categories: lone pairs of electrons are in the aromatic ring conjugated system; and lone pairs of electrons do not participate. Compound: Pyridine-3,5-dicarbonitrile, is researched, Molecular C7H3N3, CAS is 1195-58-0, about Vapor-phase oxidation and oxidative ammonolysis of some alkylpyridines on a vanadium-iron catalyst. Author is Suvorov, B. V.; Belova, N. A.; Kan, I. I.; Rakhimova, M. A..

Optimum conditions were determined for gas-phase oxidation and oxidative ammonolysis for each of 4 alkylpyridines (2- and 3-picoline, 2-methyl-5-ethylpyridine, 3,5-lutidine) over the catalyst 2V2O5·Fe2O3 in the presence or absence of H2O. At best, overall selectivity for oxygen- and nitrogen-containing derivatives (e.g., cyanopyridines) of pyridine reached 80-90%.

There is still a lot of research devoted to this compound(SMILES:N#CC1=CC(C#N)=CN=C1)Name: Pyridine-3,5-dicarbonitrile, and with the development of science, more effects of this compound(1195-58-0) can be discovered.

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