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1-(4-Fluoro-benzyl)-piperidine-4-carboxylic acid hydrochloride is a chemical compound that belongs to the class of piperidine carboxylic acid derivatives. It has a molecular formula C13H17FN2O2.HCl and a molecular weight of 290.75 g/mol. 1-(4-FLUORO-BENZYL)-PIPERIDINE-4-CARBOXYLIC ACID HYDROCHLORIDE is commonly used as a pharmaceutical intermediate in the synthesis of various drugs and active pharmaceutical ingredients. Its hydrochloride form enhances its stability, making it suitable for pharmaceutical formulations. It may also possess potential biological activities and pharmacological properties, which contribute to its importance in the development of new medications.

193538-25-9

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193538-25-9 Usage

Uses

Used in Pharmaceutical Industry:
1-(4-Fluoro-benzyl)-piperidine-4-carboxylic acid hydrochloride is used as a pharmaceutical intermediate for the synthesis of various drugs and active pharmaceutical ingredients. Its unique chemical structure and properties make it a valuable component in the development of new medications.
As a Building Block for Drug Synthesis:
1-(4-Fluoro-benzyl)-piperidine-4-carboxylic acid hydrochloride serves as a building block in the synthesis of complex drug molecules. Its presence in the molecular structure can impart specific biological activities and pharmacological properties, contributing to the therapeutic effects of the final drug product.
In Medicinal Chemistry Research:
1-(4-FLUORO-BENZYL)-PIPERIDINE-4-CARBOXYLIC ACID HYDROCHLORIDE is used in medicinal chemistry research to explore its potential as a lead compound for the development of new drugs. Its unique structure and properties can be further modified and optimized to enhance its biological activity and pharmacological profile.
For Stability and Formulation in Drug Development:
The hydrochloride form of 1-(4-Fluoro-benzyl)-piperidine-4-carboxylic acid hydrochloride provides increased stability, which is essential for pharmaceutical formulations. This stability ensures that the compound maintains its integrity and effectiveness during the manufacturing and storage processes, ultimately leading to a more reliable and consistent drug product.
In the Development of Novel Therapeutic Agents:
Due to its potential biological activities and pharmacological properties, 1-(4-Fluoro-benzyl)-piperidine-4-carboxylic acid hydrochloride is used in the development of novel therapeutic agents. Researchers can leverage its unique characteristics to create new drugs that target specific diseases or conditions, potentially leading to more effective treatments and improved patient outcomes.

Check Digit Verification of cas no

The CAS Registry Mumber 193538-25-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,3,5,3 and 8 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 193538-25:
(8*1)+(7*9)+(6*3)+(5*5)+(4*3)+(3*8)+(2*2)+(1*5)=159
159 % 10 = 9
So 193538-25-9 is a valid CAS Registry Number.

193538-25-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[(4-fluorophenyl)methyl]piperidine-4-carboxylic acid

1.2 Other means of identification

Product number -
Other names 1-(4-Fluoro-benzyl)-piperidine-4-carboxylic acid

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:193538-25-9 SDS

193538-25-9Relevant academic research and scientific papers

N-and o-substituted 4-[2-( diphenylmethoxy) -ethyl]-1- (phenyl) methyl) piperidine analogs and methods of treating cns disorders therewith

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Page 11, (2008/06/13)

N- and O-substituted 4[2-diaromaticmethoxy and methylamino)alkyl]piperidines exhibit high CNS activity with respect to the dopamine transporter (DAT) and serotonin transporter (SERT). Preferred compounds exhibit highly differential behavior as between the

Structure - Activity relationship studies of 4-[2-(diphenylmethoxy)ethyl]-1-benzylpiperidine derivatives and their N-analogues: Evaluation of behavioral activity of O- and N-analogues and their binding to monoamine transporters

Dutta,Fei,Beardsley,Newman,Reith

, p. 937 - 948 (2007/10/03)

In our effort to develop a pharmacotherapy for the treatment of cocaine addiction, we embarked on synthesizing novel molecules targeting the dopamine transporter (DAT) molecule in the brain as DAT has been implicated strongly in the reinforcing effect of

Carbamoyloxy derivatives of mutiline and their use as antibacterials

-

, (2008/06/13)

PCT No. PCT/EP96/05874 Sec. 371 Date Dec. 4, 1998 Sec. 102(e) Date Dec. 4, 1998 PCT Filed Dec. 19, 1996 PCT Pub. No. WO97/25309 PCT Pub. Date Jul. 17, 1997Derivatives of mutiline of formula (1A) and pharmaceutically acceptable salts and derivatives thereof, in which R1 is ethyl or vinyl, Y is a carbamoyloxy group, in which the N-atom is unsubstituted, or mono- or di-substituted, are useful in the treatment of bacterial infections.

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