6-Chloro-7-methylimidazo[1,2-b]pyridazine is a heterocyclic organic compound characterized by its fused imidazole and pyridazine rings, which contribute to its unique chemical properties. The presence of a chlorine atom at the 6-position and a methyl group at the 7-position of the imidazo ring influences its reactivity and potential biological activity. This compound is typically classified as a nitrogen-containing heterocycle, which can exhibit various properties such as being a potential mutagen or carcinogen, depending on its structure and substituents. Its molecular structure allows for interactions with biological macromolecules, which may lead to significant pharmacological effects. Additionally, the compound's solubility, stability, and reactivity can vary based on environmental conditions and the presence of other chemical species. As with many heterocycles, it may also participate in various chemical reactions, including electrophilic substitutions and nucleophilic attacks, making it of interest in both synthetic and medicinal chemistry. Safety and handling precautions are essential due to its potential biological implications.

6-chloro-7-methylimidazo[1,2-b]pyridazine

17412-19-0: 6-Chloro-7-methylimidazo[1,2-b]pyridazine is a heterocyclic organic compound characterized by its fused imidazole and pyridazine rings, which contribute to its unique chemical properties. The presence of a chlorine atom at the 6-position and a methyl group at the 7-position of the imidazo ring influences its reactivity and potential biological activity. This compound is typically classified as a nitrogen-containing heterocycle, which can exhibit various properties such as being a potential mutagen or carcinogen, depending on its structure and substituents. Its molecular structure allows for interactions with biological macromolecules, which may lead to significant pharmacological effects. Additionally, the compound's solubility, stability, and reactivity can vary based on environmental conditions and the presence of other chemical species. As with many heterocycles, it may also participate in various chemical reactions, including electrophilic substitutions and nucleophilic attacks, making it of interest in both synthetic and medicinal chemistry. Safety and handling precautions are essential due to its potential biological implications.

6-Chloro-7-methylimidazo[1,2-b]pyridazine

CAS 17412-19-0

6-chloro-7-methylimidazo[1,2-b]pyridazine

6-Chloro-7-methylimidazo[1,2-b]pyridazine

Ref: 54-OR1032545

6-CHLORO-7-METHYLIMIDAZO[1,2-B]PYRIDAZINE

Ref: 10-F531402

6-Chloro-7-methylimidazo[1,2-b]pyridazine

Ref: 3D-SAA41219