208511-67-5 Usage
Uses
Used in Medicinal Chemistry:
3-(4-Carboxyphenyl)pyrazole is used as a chemical intermediate for the synthesis of pharmaceutical compounds. Its unique structure allows it to interact with biological systems, making it a promising candidate for the development of new drugs.
Used in Pharmaceutical Research:
3-(4-Carboxyphenyl)pyrazole is used as a research tool in pharmaceutical research to study its potential effects on cellular processes. Its ability to influence biological systems can provide insights into the development of new therapeutic agents.
Used in Synthesis of Complex Compounds:
3-(4-Carboxyphenyl)pyrazole is used as a building block for the synthesis of more complex compounds with desirable biological activities. Its unique structure can be incorporated into larger molecules to create new compounds with potential therapeutic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 208511-67-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,8,5,1 and 1 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 208511-67:
(8*2)+(7*0)+(6*8)+(5*5)+(4*1)+(3*1)+(2*6)+(1*7)=115
115 % 10 = 5
So 208511-67-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H8N2O2/c13-10(14)8-3-1-7(2-4-8)9-5-6-11-12-9/h1-6H,(H,11,12)(H,13,14)
208511-67-5Relevant articles and documents
Benzamide nitriles
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Page 35, (2010/02/09)
Compounds of the formula (I) wherein m, n, A, R1, R2, R3, R4, R5 and R6 are as described herein, together with methods for making the compounds and using the compounds for treatment of diseases or conditions mediated by Cathepsin K.
A general, [1+4] approach to the synthesis of 3(5)-substituted pyrazoles from aldehydes
Almirante, Nicoletta,Cerri, Alberto,Fedrizzi, Giorgio,Marazzi, Giuseppe,Santagostino, Marco
, p. 3287 - 3290 (2007/10/03)
A new, one-pot preparation of 3(5)-substituted-1H-pyrazole is described that employs Horner-Emmons reaction of aldehydes with dianion of novel phosphonate 1 and proceeds through cyclization of N-sodium salt of α,β- unsaturated tosylhydrazones 2.
