135641-91-7 Usage
General Description
3-(4-Chlorophenyl)-1H-pyrazole-4-carboxylic acid is a chemical compound that belongs to the class of pyrazole carboxylic acids. It is characterized by the presence of a pyrazole ring substituted with a chlorophenyl group at the 3-position and a carboxylic acid group at the 4-position. 3-(4-CHLOROPHENYL)-1H-PYRAZOLE-4-CARBOXYLIC ACID is used in the synthesis of various pharmaceuticals and agrochemicals due to its potential as a building block for the development of new compounds with biological activities. Additionally, it has been investigated for its potential anti-inflammatory and antifungal properties, making it an important target for drug discovery and development.
Check Digit Verification of cas no
The CAS Registry Mumber 135641-91-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,6,4 and 1 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 135641-91:
(8*1)+(7*3)+(6*5)+(5*6)+(4*4)+(3*1)+(2*9)+(1*1)=127
127 % 10 = 7
So 135641-91-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H7ClN2O2/c11-7-3-1-6(2-4-7)9-8(10(14)15)5-12-13-9/h1-5H,(H,12,13)(H,14,15)
135641-91-7Relevant articles and documents
Synthesis and anti-inflammatory evaluation of some new 3,6-disubstituted-1, 2,4-triazolo-[3,4-b]-1,3,4-thiadiazoles bearing pyrazole moiety
Malladi, Shridhar,Isloor, Arun M.,Shetty, Prashanth,Fun, Hoong Kun,Telkar, Sandeep,Mahmood, Riaz,Isloor, Nishitha
, p. 3272 - 3280,9 (2020/08/20)
In the present study, a new series of 3,6-disubstituted- 1,2,4-triazolo-[3,4-b]-1,3,4-thiadiazoles (4aj) have been synthesized by condensing 3-substituted-4-amino-5- mercapto-1,2,4-triazoles (1a-b) with various 3-substitutedpyrazole- 4-carboxylic acids (3
Synthesis of 3-substituted arylpyrazole-4-carboxylic acids
Lebedev,Lebedeva,Sheludyakov,Kovaleva,Ustinova,Kozhevnikov
, p. 782 - 789 (2007/10/03)
A method was suggested for preparing previously unknown 3-aryl-substituted pyrazole-4-carboxylic acids, involving Vilsmeier formylation of semicarbazones of 26 available mono- and disubstituted acetophenones and 2-acetylthiophene followed by oxidation of
