The Instruction of (6-Chloro-pyridazin-3-yl)-piperidin-3-ylMethyl-aMine hydrochloride, 98+% C10H16Cl2N4, MW: 263.17

Instruction of (6-Chloro-pyridazin-3-yl)-piperidin-3-ylMethyl-aMine Hydrochloride: An Essential Compound in the Chemical Industry

(6-Chloro-pyridazin-3-yl)-piperidin-3-ylMethyl-aMine hydrochloride, also known by its chemical formula C10H16Cl2N4, is an important compound in the chemical industry.
This synthetic chemical compound is widely used as an intermediate in the production of various pharmaceuticals, agrochemicals, and other chemical products.

In this article, we will discuss the instruction of (6-Chloro-pyridazin-3-yl)-piperidin-3-ylMethyl-aMine hydrochloride, including its chemical structure, properties, synthesis, and uses.

Chemical Structure of (6-Chloro-pyridazin-3-yl)-piperidin-3-ylMethyl-aMine Hydrochloride

(6-Chloro-pyridazin-3-yl)-piperidin-3-ylMethyl-aMine hydrochloride is a synthetic chemical compound that belongs to the class of piperidine derivatives.
It has a unique chemical structure consisting of a six-membered aromatic ring fused to a five-membered pyrazine ring, which is further substituted with a chlorine atom.
The piperidine moiety consists of a six-membered aromatic ring that is substituted with a methylamine group.
The hydrochloride ion is attached to the nitrogen atom of the methylamine group, which makes it a salt-like compound.

Properties of (6-Chloro-pyridazin-3-yl)-piperidin-3-ylMethyl-aMine Hydrochloride

(6-Chloro-pyridazin-3-yl)-piperidin-3-ylMethyl-aMine hydrochloride is a water-insoluble, nearly colorless liquid at room temperature.
It is slightly soluble in organic solvents such as ethanol and methanol.
The compound is stable under normal storage conditions and does not exhibit any significant reactivity under normal temperature and pressure.

Synthesis of (6-Chloro-pyridazin-3-yl)-piperidin-3-ylMethyl-aMine Hydrochloride

(6-Chloro-pyridazin-3-yl)-piperidin-3-ylMethyl-aMine hydrochloride can be synthesized by various methods, depending on the intended application.
One of the most common methods involves the reaction of 3-iodo-pyridazine with methylamine hydrochloride in the presence of a solvent such as dichloromethane.

The reaction produces the intermediate compound (6-chloro-pyridazin-3-yl)methanamine, which can then be converted into (6-chloro-pyridazin-3-yl)-piperidin-3-ylMethyl-aMine hydrochloride by reacting it with piperidine in the presence of a solvent such as acetonitrile.
The resulting compound can then be purified by recrystallization or other appropriate methods.

Uses of (6-Chloro-pyridazin-3-yl)-piperidin-3-ylMethyl-aMine Hydrochloride

(6-Chloro-pyridazin-3-yl)-piperidin-3-ylMethyl-aMine hydrochloride is widely used as an