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(R)-4-(3-chloropyridin-2-yl)-N-(4-isopropylphenyl)-2-methylpiperazine-1-carboxamide is a complex organic compound characterized by a piperazine ring with a chloropyridinyl and isopropylphenyl substituent. It features a carboxamide group attached to the nitrogen of the piperazine and a methyl group at the 2-position of the piperazine ring. (R)-4-(3-chloropyridin-2-yl)-N-(4-isopropylphenyl)-2-methylpiperazine-1-carboxamide is recognized for its potential as a pharmaceutical intermediate or active ingredient in drug development, attributed to its unique molecular structure and possible biological activities. It holds promise in medicinal chemistry, particularly for the creation of innovative therapeutic agents that could target specific biological pathways or cellular receptors. Further exploration and research are essential to uncover the full spectrum of its chemical and pharmacological properties.

393514-22-2

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393514-22-2 Usage

Uses

Used in Pharmaceutical Development:
(R)-4-(3-chloropyridin-2-yl)-N-(4-isopropylphenyl)-2-methylpiperazine-1-carboxamide is utilized as a pharmaceutical intermediate for the synthesis of new drugs, leveraging its unique molecular structure to potentially interact with specific biological targets or pathways.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, (R)-4-(3-chloropyridin-2-yl)-N-(4-isopropylphenyl)-2-methylpiperazine-1-carboxamide serves as a key component in the design and development of novel therapeutic agents, aimed at treating various diseases by modulating specific cellular receptors or biological mechanisms.
Used in Drug Discovery:
(R)-4-(3-chloropyridin-2-yl)-N-(4-isopropylphenyl)-2-methylpiperazine-1-carboxamide is employed in drug discovery processes to identify new lead compounds or optimize existing drug candidates, capitalizing on its potential biological activities and chemical properties.
Used in Chemical Synthesis:
(R)-4-(3-chloropyridin-2-yl)-N-(4-isopropylphenyl)-2-methylpiperazine-1-carboxamide is also used in chemical synthesis for creating derivatives or analogs that may possess enhanced or modified pharmacological properties, contributing to the advancement of drug development and medicinal chemistry.
Note: The specific applications mentioned are hypothetical and based on the compound's potential as described in the provided materials. Actual uses would depend on the outcomes of further research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 393514-22-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,9,3,5,1 and 4 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 393514-22:
(8*3)+(7*9)+(6*3)+(5*5)+(4*1)+(3*4)+(2*2)+(1*2)=152
152 % 10 = 2
So 393514-22-2 is a valid CAS Registry Number.
InChI:InChI=1/C20H25ClN4O/c1-14(2)16-6-8-17(9-7-16)23-20(26)25-12-11-24(13-15(25)3)19-18(21)5-4-10-22-19/h4-10,14-15H,11-13H2,1-3H3,(H,23,26)/t15-/m1/s1

393514-22-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R)-4-(3-chloropyridin-2-yl)-2-methyl-N-(4-propan-2-ylphenyl)piperazine-1-carboxamide

1.2 Other means of identification

Product number -
Other names EX-8458

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:393514-22-2 SDS

393514-22-2Upstream product

393514-22-2Downstream Products

393514-22-2Relevant academic research and scientific papers

Capsaicin receptor ligands

-

, (2008/06/13)

Disclosed are diaryl piperazines and related compounds. These compounds are selective modulators of capsaicin receptors, including human capsaicin receptors, that are, therefore, useful in the treatment of a chronic and acute pain conditions, itch and urinary incontinence. Methods of treatment of such disorders and well as packaged pharmaceutical compositions are also provided. Compounds of the invention are also useful as probes for the localization of capsaicin receptors and as standards in assays for capsaicin receptor binding and capsaicin receptor mediated cation conductance. Methods of using the compounds in receptor localization studies are given.

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