885-46-1 Usage
Uses
Used in Pharmaceutical Research and Development:
5-METHYL-2-P-TOLYL-2H-PYRAZOLE-3-CARBOXYLIC ACID is used as a building block or intermediate for the synthesis of biologically active molecules, contributing to the development of new pharmaceuticals.
Used in Organic Synthesis:
5-METHYL-2-P-TOLYL-2H-PYRAZOLE-3-CARBOXYLIC ACID is used as a reagent in chemical reactions, facilitating the synthesis of various organic compounds.
Used in Chemical Reactions:
5-METHYL-2-P-TOLYL-2H-PYRAZOLE-3-CARBOXYLIC ACID is used as a reagent to catalyze or participate in chemical reactions, aiding in the production of desired products in the chemical industry.
Check Digit Verification of cas no
The CAS Registry Mumber 885-46-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,8 and 5 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 885-46:
(5*8)+(4*8)+(3*5)+(2*4)+(1*6)=101
101 % 10 = 1
So 885-46-1 is a valid CAS Registry Number.
InChI:InChI=1/C12H12N2O2/c1-8-3-5-10(6-4-8)14-11(12(15)16)7-9(2)13-14/h3-7H,1-2H3,(H,15,16)
885-46-1Relevant academic research and scientific papers
Synthesis and insecticidal evaluation of aryl pyrazole 5-fluorouracil compounds
Chen, Yue,Fu, Xiao-Dong,Mu, Hai-Ping,Qin, Xiao-Fei,Wan, Rong
, p. 272 - 279 (2014/06/09)
Twenty eight aryl pyrazole derivatives containing 5-fluorouracil were designed and synthesised via the key intermediate 1-aryl-3-methyl-1H-pyrazole-5- carboxylic acid. The structures of target compounds were confirmed by 1H NMR, FT-IR, EA and t
Microwave-assisted synthesis of tetrazolyl pyrazole amides
Hu, Jun,Wang, Jikui,Zhou, Taoyu,Xu, Yanhua
, p. 525 - 527 (2011/11/30)
A rapid and efficient microwave-assisted synthesis N-(1H-tetrazol-5-yl) derivatives of 3-methyl-1-phenyl-1H-pyrazole- 5-carboxamide is described. These tetrazole pyrazole amides have interesting bacteriocidal, pesticidal, herbicidal and antimicrobial activities. They were identified by IR and 1H NMR elemental analyses. The target compounds were obtained in a shorter reaction time compared to conventional heating methods.