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2,2,2-Trifluoro-1-[1-(4-fluorophenyl)-1H-indazol-5-yl]ethanone is a synthetic organic compound belonging to the class of indazole derivatives. It features a fluorinated ketone structure with a trifluoromethyl group attached to the carbon atom and a 4-fluorophenyl-indazole moiety. 2,2,2-Trifluoro-1-[1-(4-fluorophenyl)-1H-indazol-5-yl]ethanone holds potential in medicinal chemistry and pharmaceutical research due to its unique molecular composition, which includes fluorine and indazole components. These characteristics make it a promising candidate for drug development and exploration of its biological and pharmacological properties. However, the specific applications and effects of 2,2,2-Trifluoro-1-[1-(4-fluorophenyl)-1H-indazol-5-yl]ethanone are still under investigation and have not been fully determined.

917494-85-0

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917494-85-0 Usage

Uses

Used in Pharmaceutical Research:
2,2,2-Trifluoro-1-[1-(4-fluorophenyl)-1H-indazol-5-yl]ethanone is used as a chemical entity in pharmaceutical research for its potential role in drug development. The presence of fluorine atoms can influence the compound's lipophilicity, metabolic stability, and receptor binding properties, which are crucial factors in the design of new drugs.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 2,2,2-Trifluoro-1-[1-(4-fluorophenyl)-1H-indazol-5-yl]ethanone serves as a structural framework for the synthesis of new molecules with possible therapeutic applications. Its indazole core and fluorophenyl group may impart specific biological activities that can be further optimized through chemical modifications.
Used in Biological and Pharmacological Studies:
2,2,2-Trifluoro-1-[1-(4-fluorophenyl)-1H-indazol-5-yl]ethanone is utilized in biological and pharmacological studies to investigate its interactions with biological targets, such as enzymes, receptors, or ion channels. Understanding these interactions can provide insights into the compound's potential therapeutic effects and mechanisms of action.

Check Digit Verification of cas no

The CAS Registry Mumber 917494-85-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,7,4,9 and 4 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 917494-85:
(8*9)+(7*1)+(6*7)+(5*4)+(4*9)+(3*4)+(2*8)+(1*5)=210
210 % 10 = 0
So 917494-85-0 is a valid CAS Registry Number.

917494-85-0Relevant academic research and scientific papers

GLUCOCORTICOID MIMETICS, METHODS OF MAKING THEM, PHARMACEUTICAL COMPOSITIONS, AND USES THEREOF

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Page/Page column 117-118, (2008/06/13)

Compounds of Formula (IA) and (IB) wherein R?1?, R?2?, R?3?, A, B, C, D, and E are as defined herein, or a tautomer, prodrug, solvate, or salt thereof; pharmaceutical compositions containing such compounds, and methods of modulating the glucocorticoid receptor function and methods of treating disease-states or conditions mediated by the glucocorticoid receptor function or characterized by inflammatory, allergic, or proliferative processes in a patient using these compounds.

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