Pyridazine derivatives
Pyridazine derivatives contain a six-membered aromatic 1,2-diazine ring with adjacent nitrogen atoms. This distinguishes them from pyrazine (1,4-diazine) and pyrimidine (1,3-diazine) derivatives. Substitution or ring fusion creates distinct compounds, so identity depends on the ring system and substitution pattern.
Published research uses pyridazine cores as heterocyclic building blocks and studies their functionalisation in synthetic and medicinal chemistry. These class-level contexts do not establish common activity or end use. Compare the full name, structure, CAS number where available, molecular formula, and substituent positions. For an unlisted analogue, send an exact structure or identifier with your custom-synthesis enquiry.
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(6-Chloroimidazo[1,2-b]pyridazin-3-yl)methanol
(6-Chloroimidazo[1,2-b]pyridazin-3-yl)methanol, CAS 675580-49-1, has formula C7H6ClN3O and PubChem CID 57352521.
6-chloro-2-Methyl-3-broMo-iMidazo[1,2-b]pyridazine
Methyl 5-chloropyridazine-3-carboxylate
Methyl 5-chloropyridazine-3-carboxylate is the C6H5ClN2O2 identity linked to CAS 1256786-31-8 and PubChem CID 131699995.
3,6-Diiodopyridazine
6-iodopyridazin-3-amine
6-Iodopyridazin-3-amine, CAS 187973-60-0, formula C4H4IN3, corresponds to PubChem CID 10867834.
5,6-dihydropyridazin-4-ol
2-Amino-6-chloroimidazo[1,2-b]pyridazine
6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridazin-3-amine
5,6-Dichloro-4-pyridazinecarbonitrile
3-Methylpyridazin-4-amine