381229-48-7 Usage
Uses
Used in Pharmaceutical Industry:
3-Chloro-4-fluoro-5-(trifluoromethyl)benzoic acid is used as an intermediate in the synthesis of pharmaceuticals for its ability to introduce specific functional groups into organic molecules, which can enhance the pharmacological properties of the final drug product.
Used in Agrochemical Industry:
3-Chloro-4-fluoro-5-(trifluoromethyl)benzoic acid is used as an intermediate in the synthesis of agrochemicals, contributing to the development of new compounds with potential applications in agriculture, such as pesticides and herbicides.
Used in Organic Chemistry:
3-Chloro-4-fluoro-5-(trifluoromethyl)benzoic acid is used as a building block in the production of other specialty chemicals, playing a crucial role in the synthesis of complex organic molecules with specific properties.
Used in Research and Development:
3-Chloro-4-fluoro-5-(trifluoromethyl)benzoic acid is used as a research tool in the development of new compounds with potential pharmacological activities, aiding scientists in exploring novel therapeutic agents and chemical reactions.
Check Digit Verification of cas no
The CAS Registry Mumber 381229-48-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,8,1,2,2 and 9 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 381229-48:
(8*3)+(7*8)+(6*1)+(5*2)+(4*2)+(3*9)+(2*4)+(1*8)=147
147 % 10 = 7
So 381229-48-7 is a valid CAS Registry Number.
381229-48-7Relevant academic research and scientific papers
Heteroaryl and benzyl amide compounds
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Page/Page column 17, (2010/11/28)
Compounds of formula I wherein R1, R2, R4, R5, A, B, D and n are as defined, and pharmaceutically acceptable salts thereof, processes for their preparation, their use as pharmaceuticals and pharmaceutical compositions comprising them.
Discovery of novel p-arylthio cinnamides as antagonists of leukocyte function-associated antigen-1/intercellular adhesion molecule-1 interaction. 4. Structure - Activity relationship of substituents on the benzene ring of the cinnamide
Winn,Kester,Von Geldern,Leitza,Devries,Dickinson,Mussatto,Okasinski,Reilly,Liu,Huth,Jae,Freeman,Pei,Xin,Lynch
, p. 4393 - 4403 (2007/10/03)
We have shown that p-arylthio cinnamides can inhibit the interaction of LFA-1 and ICAM-1, which is involved in cell adhesion and the inflammatory process. We now show that 2,3-disubstitution on the aryl portion of the cinnamide results in enhanced activit
