
Piperidin-3-one Hydrochloride CAS 61644-00-6
What is Piperidin-3-one Hydrochloride CAS 61644-00-6?
Piperidin-3-one hydrochloride is an organic solvent that belongs to the group of benzyl compounds. It is a reagent for the synthesis of sulfides, which are used in the production of dyes, pharmaceuticals, and other products. Piperidin-3-one hydrochloride can be used as a constant in calculating the shift of tetrafluoroborate ions.
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Features of Piperidin-3-one Hydrochloride CAS 61644-00-6
Here are some features of piperidin-3-one hydrochloride, also known as 3-piperidone hydrochloride, with the CAS number 61644-00-6:
Molecular formula: C5H9NO·HCl
Molecular weight: 135.61
Boiling point: 220°C at 760 mmHg
Flash point: 86.8°C
LOGP: 1.06970
Scientific Research Applications of Piperidin-3-one hydrochloride
Piperidin-3-one hydrochloride has a wide range of applications in scientific research:
Chemistry
It is used as a building block in the synthesis of complex organic molecules.
01
Biology
It is used in the study of enzyme mechanisms and protein-ligand interactions.
02
Medicine
It is a key intermediate in the synthesis of various pharmaceuticals, including analgesics, antipsychotics, and antihypertensives.
03
Industry
It is used in the production of agrochemicals and other industrial chemicals.
04
Biochemical Properties
Piperidin-3-one hydrochloride plays a vital role in biochemical reactions. It interacts with various enzymes, proteins, and other biomolecules. For instance, it is used as a reactant in the preparation of quinolines and quinazolines, which are employed in the treatment of benign prostatic hyperplasia . The compound's interactions with these biomolecules are primarily through hydrogen bonding and hydrophobic interactions, which facilitate the formation of stable complexes essential for therapeutic applications.
Cellular Effects
This compound has been shown to influence various cellular processes. It affects cell signaling pathways, gene expression, and cellular metabolism. For example, piperidine derivatives have demonstrated significant antitumor properties against various cancer cell lines, including HCT-116, T-47D, HL-60, MOLT-4, RPMI-8226, and PC-3 . These effects are mediated through the modulation of cell signaling pathways and the regulation of gene expression, leading to altered cellular metabolism and reduced proliferation of cancer cells.
Molecular Mechanism
The molecular mechanism of action of this compound involves its binding interactions with biomolecules, enzyme inhibition or activation, and changes in gene expression. Piperidine derivatives have been found to exhibit dual cholinesterase inhibition and target the beta-secretase enzyme . These interactions result in the inhibition of enzyme activity, leading to the accumulation of specific substrates and subsequent changes in cellular function.
Temporal Effects in Laboratory Settings
In laboratory settings, the effects of this compound change over time. The compound's stability and degradation are critical factors influencing its long-term effects on cellular function. Studies have shown that piperidine derivatives exhibit both antiaggregatory and antioxidant effects over time . These properties contribute to the compound's therapeutic potential and its ability to maintain efficacy in long-term applications.
Dosage Effects in Animal Models
The effects of this compound vary with different dosages in animal models. At lower doses, the compound exhibits therapeutic effects, such as antipsychotic activity with limited adverse effects . At higher doses, toxic or adverse effects may be observed, including neurotoxicity and hepatotoxicity. These threshold effects highlight the importance of dosage optimization in preclinical studies to ensure safety and efficacy.
Metabolic Pathways
This compound is involved in various metabolic pathways. It interacts with enzymes and cofactors that facilitate its conversion into active metabolites. For instance, the compound undergoes hydrogenation and cyclization reactions to form piperidine rings, which are crucial for its biological activity . These metabolic pathways influence the compound's pharmacokinetics and its overall therapeutic potential.
Transport and Distribution
The transport and distribution of this compound within cells and tissues are mediated by specific transporters and binding proteins. These interactions determine the compound's localization and accumulation in target tissues. Piperidine derivatives have been shown to exhibit good bioavailability and tissue distribution, which are essential for their therapeutic efficacy .
Subcellular Localization
This compound's subcellular localization affects its activity and function. The compound is directed to specific compartments or organelles through targeting signals and post-translational modifications. These processes ensure that the compound reaches its site of action and exerts its therapeutic effects. Piperidine derivatives have been found to localize in the cytoplasm and nucleus, where they modulate cellular processes and gene expression .
Biosynce have an independent R&D and inspection center to strictly test the quality of products and provide customers with high quality products, our products are widely exported to North America, Europe, Asia and Africa. We aim to establish long-term and mutually beneficial relationships with customers and offer excellent products and services.

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