《Pyridazine analogs of biologically active compounds. VI. Pyrido[2,3-c]pyridazines structurally related to nalidixic acid》 was written by Boamah, Philip Y.; Haider, Norbert; Heinisch, Gottfried. Safety of 3-Chloropyridazine-4-carbonitrile And the article was included in Archiv der Pharmazie (Weinheim, Germany) on April 30 ,1990. The article conveys some information:
Synthesis of 8-alkyl-5,8-dihydro-5-oxopyrido[2,3-c]pyridazine-6-carboxylic acids I (R = Et, Pr, Me2CH, cyclopropyl) starting from 3-chloro-4-pyridazinecarbonitrile is reported. I do not exhibit significant (gyrase-inhibiting) antibacterial activity. In addition to this study using 3-Chloropyridazine-4-carbonitrile, there are many other studies that have used 3-Chloropyridazine-4-carbonitrile(cas: 1445-56-3Safety of 3-Chloropyridazine-4-carbonitrile) was used in this study.
3-Chloropyridazine-4-carbonitrile(cas: 1445-56-3) 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.Safety of 3-Chloropyridazine-4-carbonitrile
Referemce:
Pyridazine – Wikipedia,
Pyridazine | C4H4N2 – PubChem