Electronic structure and spectra of organic molecules. XVI. Amine-imine tautomerism in azines substituted by amino groups was written by Kwiatkowski, J. S.. And the article was included in Acta Physica Polonica, A in 1972.Recommanded Product: 3-Aminopyridazine This article mentions the following:
For both amine and imine tautomers of amine-substituted pyridines and diazines, Pariser-Parr-Pople type calculations (K., 1970) gave singlet-singlet transition energies which agreed with exptl. data. In all cases, the singlet-singlet transitions of the imine forms red shifted relative to the corresponding transitions of the amine forms. In the experiment, the researchers used many compounds, for example, 3-Aminopyridazine (cas: 5469-70-5Recommanded Product: 3-Aminopyridazine).
3-Aminopyridazine (cas: 5469-70-5) belongs to pyridazine derivatives. The pyridazine structure is a popular pharmacophore which is found within a number of herbicides such as credazine, pyridafol and pyridate. Pyridazine compounds have attracted interest in various fields like medicinal, industrial, and agricultural research as they are used for numerous biological activities and other applications.Recommanded Product: 3-Aminopyridazine
Referemce:
Pyridazine – Wikipedia,
Pyridazine | C4H4N2 – PubChem