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1-(4-Fluoro-benzoyl)-piperidine-4-carboxylic acid is a chemical compound with the molecular formula C16H17NO3F. It is a piperidine derivative featuring a carboxylic acid group and a fluorobenzoyl group attached to the piperidine ring. 1-(4-FLUORO-BENZOYL)-PIPERIDINE-4-CARBOXYLIC ACID is known for its potential applications in the synthesis of pharmaceuticals and other organic molecules, as well as its possible utility in medicinal chemistry and drug discovery due to its unique structural features. It may also exhibit biological activity, making it a compound of interest to researchers in the fields of organic chemistry and drug development.

139679-45-1

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139679-45-1 Usage

Uses

Used in Pharmaceutical Synthesis:
1-(4-Fluoro-benzoyl)-piperidine-4-carboxylic acid is used as a building block in the synthesis of pharmaceuticals and other organic molecules. Its unique structure allows it to be a valuable component in creating new compounds with potential therapeutic properties.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 1-(4-Fluoro-benzoyl)-piperidine-4-carboxylic acid is used as a starting material for the development of new drugs. Its structural features make it a promising candidate for the design and synthesis of molecules with specific biological activities.
Used in Drug Discovery:
1-(4-Fluoro-benzoyl)-piperidine-4-carboxylic acid may have potential applications in drug discovery due to its structural features. Researchers can use 1-(4-FLUORO-BENZOYL)-PIPERIDINE-4-CARBOXYLIC ACID to explore new avenues in the development of therapeutic agents, particularly those targeting specific biological pathways or receptors.
Used in Organic Chemistry Research:
In the realm of organic chemistry, 1-(4-Fluoro-benzoyl)-piperidine-4-carboxylic acid is used as a subject of study for understanding the properties and reactivity of compounds with similar structures. This can lead to advancements in synthetic methods and the discovery of new chemical reactions.
Used in Drug Development:
Due to its potential biological activity, 1-(4-Fluoro-benzoyl)-piperidine-4-carboxylic acid is of interest to researchers in drug development. It may serve as a lead compound or a template for the creation of new pharmaceuticals with improved efficacy, safety, or selectivity in treating various diseases and conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 139679-45-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,9,6,7 and 9 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 139679-45:
(8*1)+(7*3)+(6*9)+(5*6)+(4*7)+(3*9)+(2*4)+(1*5)=181
181 % 10 = 1
So 139679-45-1 is a valid CAS Registry Number.
InChI:InChI=1/C13H14FNO3/c14-11-3-1-9(2-4-11)12(16)15-7-5-10(6-8-15)13(17)18/h1-4,10H,5-8H2,(H,17,18)

139679-45-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-fluorobenzoyl)piperidine-4-carboxylic acid

1.2 Other means of identification

Product number -
Other names -

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:139679-45-1 SDS

139679-45-1Relevant academic research and scientific papers

Exploration of novel piperazine or piperidine constructed non-covalent peptidyl derivatives as proteasome inhibitors

Zhuang, Rangxiao,Gao, Lixin,Lv, Xiaoqing,Xi, Jianjun,Sheng, Li,Zhao, Yanmei,He, Ruoyu,Hu, Xiaobei,Shao, Yidan,Pan, Xuwang,Liu, Shourong,Huang, Weiwei,Zhou, Yubo,Li, Jia,Zhang, Jiankang

, p. 1056 - 1070 (2017)

A series of novel piperazine or piperidine-containing non-covalent peptidyl derivatives possessing a neopentyl-asparagine residue were designed, synthesized and evaluated as proteasome inhibitors. All target compounds were screened for their 20S proteasom

TETRAZINES FOR HIGH CLICK CONJUGATION YIELD IN VIVO AND HIGH CLICK RELEASE YIELD

-

Page/Page column 199, (2019/11/19)

Disclosed herein are tetrazines substituted with groups that result in a high click conjugation yield in vivo and high click release yields. In one aspect, the invention relates to kits comprising said tetrazines and a dienophile, preferably a trans-cyclo

Imidazolylbenzoyl substituted heterocycles

-

, (2008/06/13)

Novel imidazolybenzoyl substituted heterocycles and their use as cardiovascular agents most especially as Class III antiarrhythmic agents is described. Pharmaceutical formulations containing such compounds are also discussed.

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