Application In Synthesis of Pyridine-3,5-dicarbonitrile. The reaction of aromatic heterocyclic molecules with protons is called protonation. Aromatic heterocycles are more basic than benzene due to the participation of heteroatoms. Compound: Pyridine-3,5-dicarbonitrile, is researched, Molecular C7H3N3, CAS is 1195-58-0, about Dihydropyridines. XVII. π-Electronic structure and reactivity of alkyl 3,5-dicyanopyridines. Author is Kuthan, Josef; Prochazkova, J..
The π-electronic structure of alkyl 3,5-dicyanopyridines was studied by the Hueckel M.O. L.C.A.O. method. The heteroatom model was used in the calculations The exptl. course of nucleophilic reactions was in agreement with the calculated superdelocalizabilities. Some of the exptl. excitation energies depended linearly on the calculated transition energies. Correlation was found between the values of proton shifts in the N.M.R. spectra of dicyanopyridines and the corresponding electron densities.
Compound(1195-58-0)Application In Synthesis of Pyridine-3,5-dicarbonitrile received a lot of attention, and I have introduced some compounds in other articles, similar to this compound(Pyridine-3,5-dicarbonitrile), if you are interested, you can check out my other related articles.
Reference:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts