102243-12-9 Usage
Uses
Used in Pharmaceutical Industry:
2-Chloro-6-(trifluoromethyl)nicotinic acid serves as a crucial building block in the synthesis of a wide range of drugs and pharmaceutical products. Its unique structure allows for the development of new therapeutic agents with improved efficacy and safety profiles.
Used in Research and Development:
As a research tool, 2-Chloro-6-(trifluoromethyl)nicotinic acid aids in the study of various biological processes. Its presence can help researchers understand the mechanisms of action and potential interactions with biological targets, contributing to the advancement of medical knowledge.
Used as an Intermediate in Organic Synthesis:
In the realm of organic synthesis, 2-Chloro-6-(trifluoromethyl)nicotinic acid acts as an intermediate, enabling the production of more complex organic compounds. Its versatility in chemical reactions makes it a valuable component in the synthesis of various organic molecules.
Used in Therapeutic Applications:
2-Chloro-6-(trifluoromethyl)nicotinic acid has been studied for its potential therapeutic properties, including anti-inflammatory and anti-tumor activities. Its ability to modulate biological processes and target specific pathways makes it a promising candidate for the development of new treatments for various diseases.
Check Digit Verification of cas no
The CAS Registry Mumber 102243-12-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,2,4 and 3 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 102243-12:
(8*1)+(7*0)+(6*2)+(5*2)+(4*4)+(3*3)+(2*1)+(1*2)=59
59 % 10 = 9
So 102243-12-9 is a valid CAS Registry Number.
InChI:InChI=1/C15H10ClFO/c16-14-4-2-1-3-11(14)7-10-15(18)12-5-8-13(17)9-6-12/h1-10H/b10-7+
102243-12-9Relevant academic research and scientific papers
SUBSTITUTED PIPERAZINE COMPOUNDS AND METHODS AND USE THEREOF
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Paragraph 00239; 00362, (2015/11/27)
Provided herein are novel piperazine compounds acting as selective serotonin reuptake inhibitors and/or the 5-HT1A receptor agonists. The invention also relates to the methods of preparing the compound and pharmaceutical composition, and the use of treating central nervous system dysfunction in mammals especially in humans.
Synthesis and antitumor activity of ureas containing pyrimidinyl group
Jin, Chuanfei,Liang, Yong-Ju,He, Hongwu,Fu, Liwu
experimental part, p. 429 - 432 (2011/02/25)
A novel series of ureas containing pyrimidinyl group were designed and synthesized. Some of the prepared compounds showed potential cytotoxicity against several human cancer cell lines. From the structure-activity relationships we may conclude that introd
Acylaminoaryloxy and arylthio pyrimidines as herbicides
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, (2008/06/13)
As new compounds, acylaminoaryloxy and arylthio pyrimidines having the formula STR1 wherein A is oxygen or sulfur; M is CH or N; X is hydrogen, lower alkyl, halo, methoxy, alkoxy, C1 -C3 alkylthio, cyano, carbomethoxy or trifluoromet
