14174-92-6

Basic information

• Product Name: 2-(2-METHYLPHENYL)PIPERIDINE HYDROCHLORIDE
• Synonyms: 2-(2-METHYLPHENYL)PIPERIDINE HYDROCHLORIDE;2-(o-tolyl)piperidine hydrochloride
• CAS NO: 14174-92-6
• Molecular Formula: C₁₂H₁₇N*ClH
• Molecular Weight: 211.73
• Mol File: 14174-92-6.mol
• Article Data: 0

Chemical Properties

• Melting Point: 221-224 °C
• Appearance: /
• CAS DataBase Reference: 2-(2-METHYLPHENYL)PIPERIDINE HYDROCHLORIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2-METHYLPHENYL)PIPERIDINE HYDROCHLORIDE(14174-92-6)
• EPA Substance Registry System: 2-(2-METHYLPHENYL)PIPERIDINE HYDROCHLORIDE(14174-92-6)

Safety Data

• Hazard Codes: Xi
• HazardClass: IRRITANT
• Hazardous Substances Data: 14174-92-6(Hazardous Substances Data)

Usage

Description

2-(2-methylphenyl)piperidine hydrochloride is a hydrochloride salt form of 2-(2-methylphenyl)piperidine, a piperidine derivative with applications in research and pharmaceuticals. It functions as a selective dopamine autoreceptor antagonist and has been investigated for its potential therapeutic uses.

Uses

Used in Pharmaceutical Research and Development:
2-(2-methylphenyl)piperidine hydrochloride is used as a research compound for studying its effects on dopamine autoreceptors, which could lead to advancements in the treatment of various psychiatric disorders.
Used in the Treatment of Cocaine Addiction:
2-(2-methylphenyl)piperidine hydrochloride is used as a potential therapeutic agent for cocaine addiction, leveraging its properties as a selective dopamine autoreceptor antagonist to address the underlying neurochemical imbalances associated with addiction.
Used in Psychiatry:
2-(2-methylphenyl)piperidine hydrochloride is used as a candidate for the development of treatments for other psychiatric disorders, given its interaction with dopamine autoreceptors, which play a crucial role in mood regulation and cognitive function.
Used as a Local Anesthetic:
2-(2-methylphenyl)piperidine hydrochloride is used as a potential local anesthetic, taking advantage of its ability to block nerve conduction and provide pain relief during medical procedures.

Downstream Products

• 1373314-03-4 (5-fluoro-1,3-dimethyl-1H-pyrazol-4-yl)[2-(2-methylphenyl)piperidin-1-yl]methanone