447406-52-2 Usage
Uses
Used in Organic Synthesis:
2-(4-TRIFLUOROMETHYLPHENYL)THIAZOLE-5-CARBALDEHYDE is used as a key intermediate in the synthesis of various organic compounds. Its carbaldehyde group allows for a wide range of chemical reactions, such as condensation, oxidation, and reduction, enabling the formation of diverse molecular structures.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 2-(4-TRIFLUOROMETHYLPHENYL)THIAZOLE-5-CARBALDEHYDE is used as a building block for the development of new drugs. Its unique structure and functional groups can be utilized to design and synthesize bioactive molecules with potential therapeutic applications. 2-(4-TRIFLUOROMETHYLPHENYL)THIAZOLE-5-CARBALDEHYDE's reactivity and properties make it an attractive target for the discovery of novel drug candidates.
Used in Medicinal Chemistry:
2-(4-TRIFLUOROMETHYLPHENYL)THIAZOLE-5-CARBALDEHYDE is employed as a versatile scaffold in medicinal chemistry. Its thiazole ring and 4-trifluoromethylphenyl substitution provide opportunities for structural modifications and optimization of biological activity. Researchers can explore its potential as a lead compound for the development of new therapeutic agents.
Used in Material Science:
In the field of material science, 2-(4-TRIFLUOROMETHYLPHENYL)THIAZOLE-5-CARBALDEHYDE can be used as a component in the design and synthesis of novel materials with specific properties. Its unique structure and functional groups may contribute to the development of advanced materials for various applications, such as sensors, catalysts, or functional coatings.
Check Digit Verification of cas no
The CAS Registry Mumber 447406-52-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,7,4,0 and 6 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 447406-52:
(8*4)+(7*4)+(6*7)+(5*4)+(4*0)+(3*6)+(2*5)+(1*2)=152
152 % 10 = 2
So 447406-52-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H6F3NOS/c12-11(13,14)8-3-1-7(2-4-8)10-15-5-9(6-16)17-10/h1-6H
447406-52-2Relevant academic research and scientific papers
Direct Formic Acid Mediated Z-Selective Reductive Coupling of Dienes and Aldehydes
Cooze, Christopher,Dada, Raphael,Lundgren, Rylan J.
supporting information, p. 12246 - 12251 (2019/08/01)
Methods for the addition of unsaturated nucleophiles to carbonyls to generate Z-olefin products remain rare and often require either alkyl borane or zinc reductants, limiting their utility. Demonstrated here is that formic acid mediates the Rh-catalyzed,
BENZOAZEPIN-OXY-ACETIC ACID DERIVATIVES AS PPAR-DELTA AGONISTS USED FOR THE INCREASE OF HDL-C, LOWER LDL-C AND LOWER CHOLESTEROL
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Page/Page column 51-52, (2008/06/13)
The invention is directed to compounds of Formula (I) useful as PPAR agonists. Pharmaceutical compositions and methods of treating one or more conditions including, but not limited to, diabetes, nephropathy, neuropathy, retinopathy, polycystic ovary syndr
