1-(6-Chloro-pyridazino-3-yl)piperidine is a chemical compound characterized by its unique structure, which includes a piperidine ring and a pyridazino moiety. The presence of a chlorine atom at the 6-position of the pyridazine ring contributes to its reactivity and potential biological activity. This compound is typically classified as a heterocyclic organic compound, and its molecular structure suggests it may exhibit properties relevant to medicinal chemistry, particularly in the development of pharmaceuticals. The piperidine ring is known for its role in various biological activities, and the substitution on the pyridazine ring can influence the compound's pharmacological profile. Additionally, the compound's solubility, stability, and interaction with biological targets can vary based on its specific functional groups and overall molecular geometry. As with many heterocycles, it may also participate in various chemical reactions, making it of interest in synthetic organic chemistry. Safety and handling precautions should be observed due to the presence of chlorine, which can pose health risks.

1-(6-Chloro-pyridazino-3-yl)piperidine

1722-11-8: 3-Chloro-6-Piperidin-1-Ylpyridazine Hydrochloride, 3-Chloro-6-piperidin-1-yl-pyridazine, 

3-Chloro-6-piperidin-1-yl-pyridazine

3-Chloro-6-(1-piperidinyl)pyridazine is a coordination complex that is immobilized on zeolites. It can be used to remove ionic contaminants from wastewater by exchanging them for the metal ions in the coordination complex. 3-Chloro-6-(1-piperidinyl)pyridazine is also catalytic and can be used for liquid phase reactions. This ligand has been shown to have a cyclic structure and it has been modified with various substituents to change its properties, such as viscosity.

CAS 1722-11-8: 1-(6-Chloro-pyridazino-3-yl)piperidine

3-Chloro-6-piperidin-1-yl-pyridazine

Ref: 10-F033526

3-Chloro-6-(1-piperidinyl)pyridazine

Ref: 3D-FC53919

1-(6-Chloro-pyridazino-3-yl)piperidine

Ref: IN-DA003J9T

3-Chloro-6-(piperidin-1-yl)pyridazine

Ref: 54-OR959487