The chemical substance known as (2-Methyl-1-piperidinyl)(4,5,6,7-tetrahydro-1H-pyrazolo[4,3-c]pyridin-3-yl)methanone hydrochloride, with the CAS number 1220034-03-6, is a synthetic compound that features a complex molecular structure. It contains a piperidine ring, which is a six-membered nitrogen-containing heterocycle, and a tetrahydro-pyrazolo-pyridine moiety, indicating the presence of multiple fused rings. This compound is typically characterized by its potential biological activity, which may include interactions with various receptors or enzymes, making it of interest in medicinal chemistry and drug development. The hydrochloride salt form suggests enhanced solubility in aqueous solutions, which is advantageous for pharmacological applications. Additionally, the presence of the methyl group on the piperidine ring may influence its lipophilicity and overall pharmacokinetic properties. As with many synthetic organic compounds, its stability, reactivity, and specific applications would depend on the context of its use in research or therapeutic settings.

(2-Methyl-1-piperidinyl)(4,5,6,7-tetrahydro-1H-pyrazolo[4,3-c]pyridin-3-yl)methanone HCl

1220034-03-6: The chemical substance known as (2-Methyl-1-piperidinyl)(4,5,6,7-tetrahydro-1H-pyrazolo[4,3-c]pyridin-3-yl)methanone hydrochloride, with the CAS number 1220034-03-6, is a synthetic compound that features a complex molecular structure. It contains a piperidine ring, which is a six-membered nitrogen-containing heterocycle, and a tetrahydro-pyrazolo-pyridine moiety, indicating the presence of multiple fused rings. This compound is typically characterized by its potential biological activity, which may include interactions with various receptors or enzymes, making it of interest in medicinal chemistry and drug development. The hydrochloride salt form suggests enhanced solubility in aqueous solutions, which is advantageous for pharmacological applications. Additionally, the presence of the methyl group on the piperidine ring may influence its lipophilicity and overall pharmacokinetic properties. As with many synthetic organic compounds, its stability, reactivity, and specific applications would depend on the context of its use in research or therapeutic settings.

CAS 1220034-03-6

(2-Methyl-1-piperidinyl)(4,5,6,7-tetrahydro-1H-pyrazolo[4,3-c]pyridin-3-yl)methanone HCl