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4-(3-Chlorophenyl)piperidine hydrochloride is a piperidine derivative with a 3-chlorophenyl substituent, belonging to the piperidine class of organic compounds. It is commonly used in research and pharmaceutical applications as a hydrochloride salt form. Known for its action as a dopamine receptor ligand, 4-(3-CHLOROPHENYL)PIPERIDINE HYDROCHLORIDE has been studied for its potential therapeutic effects on neurological and psychiatric disorders, as well as its role in treating drug addiction and related disorders. Furthermore, it serves as a building block in the synthesis of various pharmaceuticals and research chemicals.

99329-70-1

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99329-70-1 Usage

Uses

Used in Pharmaceutical Research and Development:
4-(3-Chlorophenyl)piperidine hydrochloride is used as a research chemical for the development of new drugs, particularly those targeting dopamine receptors. Its interaction with these receptors makes it a valuable compound in the study and treatment of neurological and psychiatric disorders.
Used in Neurological and Psychiatric Disorders Treatment:
In the field of neurology and psychiatry, 4-(3-CHLOROPHENYL)PIPERIDINE HYDROCHLORIDE is used as a therapeutic agent for its potential effects on various disorders. Its modulation of dopamine receptors could contribute to the management of conditions such as schizophrenia, Parkinson's disease, and addiction.
Used in Drug Addiction Treatment:
4-(3-Chlorophenyl)piperidine hydrochloride is used as a potential treatment for drug addiction and related disorders. Its influence on dopamine pathways, which are often implicated in addiction, positions it as a candidate for further research and development in addiction medicine.
Used in Chemical Synthesis:
In the chemical synthesis industry, 4-(3-CHLOROPHENYL)PIPERIDINE HYDROCHLORIDE is used as a building block for the creation of other pharmaceuticals and research chemicals. Its structural properties allow it to be a versatile component in the synthesis of a range of compounds with diverse applications.

Check Digit Verification of cas no

The CAS Registry Mumber 99329-70-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,3,2 and 9 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 99329-70:
(7*9)+(6*9)+(5*3)+(4*2)+(3*9)+(2*7)+(1*0)=181
181 % 10 = 1
So 99329-70-1 is a valid CAS Registry Number.
InChI:InChI=1/C11H14ClN.ClH/c12-11-3-1-2-10(8-11)9-4-6-13-7-5-9;/h1-3,8-9,13H,4-7H2;1H

99329-70-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(3-Chlorophenyl)piperidine hydrochloride

1.2 Other means of identification

Product number -
Other names 4-(3-chlorophenyl)piperidine,hydrochloride

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:99329-70-1 SDS

99329-70-1Downstream Products

99329-70-1Relevant academic research and scientific papers

Synthesis and SAR study of 4-arylpiperidines and 4-aryl-1,2,3,6- tetrahydropyridines as 5-HT2C agonists

Conway, Richard J.,Valant, Celine,Christopoulos, Arthur,Robertson, Alan D.,Capuano, Ben,Crosby, Ian T.

supporting information; experimental part, p. 2560 - 2564 (2012/05/05)

A series of substituted 4-arylpiperidines and a smaller family of 4-aryl-1,2,3,6-tetrahydropyridines were synthesized and their biological activity at the 5-HT2C receptor studied to determine whether either series showed noteworthy agonist activity. Structure-activity relationships were developed from the performed receptor binding assays and functional studies, and the results of the analysis are presented herein.

GAMMA-AMINOAMIDE MODULATORS OF CHEMOKINE RECEPTOR ACTIVITY

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Page/Page column 67, (2010/02/07)

The present invention is directed to compounds of the formula (I), wherein R1, R2, R3, R4, R5, R6, R7, R8, R11, R12, W, X, and n are defined herein, which are useful as modulators of chemokine receptor activity. In particular, these compounds are useful as modulators of the chemokine receptor CCR-2.

Synthesis of piperidine analogs of 1-(3- chlorophenyl)piperazine, a well known serotonin ligand

Radl, Stanislav,Hezky, Petr,Taimr, Jan,Proska, Jan,Krejci, Ivan

, p. 1017 - 1022 (2007/10/03)

Synthesis of arylpiperideines 3a-3d and arylpiperidines 4a- 4d as analogs of a well known serotonin ligand 1-(3- chlorophenyl)piperazine is reported. Starting aryllithium derivatives were treated with 1-methyl-piperdin-4-one to provide the corresponding hydroxy derivatives 6a and 6b. N- Methylpiperideine derivatives 3a and 3c were obtained by their dehydration while the corresponding N-unsubstituted compounds 3b and 3d were prepared indirectly by a three-step procedure. Hydrogenation of piperideine 3a provided the corresponding piperidine derivative 4a which after demethylation yielded 4b. Similar 4-pyridyl derivatives 4c and 4d were prepared by a similar strategy via the corresponding methoxy derivatives.

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