1020237-74-4 Usage
Uses
Used in Pharmaceutical Industry:
1-(2-CHLORO-PHENYL)-5-TRIFLUOROMETHYL-1H-PYRAZOLE-4-CARBOXYLIC ACID ETHYL ESTER is used as a building block for the synthesis of bioactive molecules due to its unique chemical structure. Its potential in creating new pharmaceutical compounds makes it a valuable target for research and development.
Used in Agrochemical Industry:
1-(2-CHLORO-PHENYL)-5-TRIFLUOROMETHYL-1H-PYRAZOLE-4-CARBOXYLIC ACID ETHYL ESTER is used as a potential candidate for the development of new pesticides. Its structural features suggest that it may possess pesticidal properties, which warrant further investigation and development for use in agriculture.
Check Digit Verification of cas no
The CAS Registry Mumber 1020237-74-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,0,2,3 and 7 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1020237-74:
(9*1)+(8*0)+(7*2)+(6*0)+(5*2)+(4*3)+(3*7)+(2*7)+(1*4)=84
84 % 10 = 4
So 1020237-74-4 is a valid CAS Registry Number.
1020237-74-4Relevant academic research and scientific papers
Synthesis, Biological Evaluation, and 3D-QSAR Studies of N-(Substituted pyridine-4-yl)-1-(substituted phenyl)-5-trifluoromethyl-1 H-pyrazole-4-carboxamide Derivatives as Potential Succinate Dehydrogenase Inhibitors
Wu, Zhibing,Park, Hyung-Yeon,Xie, Dewen,Yang, Jingxin,Hou, Shuaitao,Shahzad, Nasir,Kim, Chan Kyung,Yang, Song
, p. 1214 - 1223 (2021/02/06)
A series of new fungicides that can inhibit the succinate dehydrogenase (SDH) was classified and named as SDH inhibitors by the Fungicide Resistance Action Committee in 2009. To develop more potential SDH inhibitors, we designed and synthesized a novel se
Method for synthesizing 1-substituted phenyl-5-trifluoromethyl (difluoromethyl)-4-pyrazole carboxylic acid
-
, (2018/01/11)
The invention relates to a method for synthesizing 1-substituted phenyl-5-trifluoromethyl (difluoromethyl)-4-pyrazole carboxylic acid. The method is as follows: performing a ring-forming reaction of phenylhydrazine or substituted phenylhydrazine with inte
