473416-82-9 Usage
Uses
Used in Pharmaceutical Industry:
1H-Indazole-5-carboxylic acid, 4-fluoro-, methyl ester is used as a chemical intermediate for the synthesis of new drugs. Its unique structure, including the heterocyclic core and the fluorine atom, may contribute to the development of pharmaceuticals with novel therapeutic properties.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, 1H-Indazole-5-carboxylic acid, 4-fluoro-, methyl ester serves as a valuable research compound. It can be utilized to explore the effects of structural modifications on the biological activity of drug candidates, potentially leading to the discovery of more effective and safer medications.
Used in Drug Design and Optimization:
1H-Indazole-5-carboxylic acid, 4-fluoro-, methyl ester is employed in drug design and optimization processes, where its properties can be leveraged to improve the pharmacokinetics, pharmacodynamics, and overall efficacy of drug molecules. The 4-fluoro substituent may play a crucial role in fine-tuning these properties, making it a promising candidate for further investigation in drug development programs.
Check Digit Verification of cas no
The CAS Registry Mumber 473416-82-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,3,4,1 and 6 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 473416-82:
(8*4)+(7*7)+(6*3)+(5*4)+(4*1)+(3*6)+(2*8)+(1*2)=159
159 % 10 = 9
So 473416-82-9 is a valid CAS Registry Number.
473416-82-9Relevant academic research and scientific papers
PYRAZOLE COMPOUND AND MEDICINAL COMPOSITION CONTAINING THE SAME
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Page/Page column 86, (2008/06/13)
The present invention provides a novel compound having an excellent JNK inhibitory effect. That is, it provides a compound represented by the following formula, a salt thereof or a hydrate of them. Wherein R1 designates -(CO)h-(NRa)j-(CRb=CRc)k-Ar (wherein Ra, Rb and Rc each independently designate a hydrogen atom, a halogen atom, hydroxyl group, an optionally substituted C1-6 alkyl group or the like; Cy designates a 5- or 6-membered heteroaryl; and V each independently designate the formula -L-X-Y (wherein L designates a single bond, an optionally substituted C1-6 alkylene group or the like; X designates a single bond or the formula -A- (wherein A designates NR2, O, CO, S, SO or SO2) and so on; and Y designates a hydrogen atom, a halogen atom, nitro group or the like).
