98534-74-8 Usage
Uses
Used in Pharmaceutical Industry:
Ethyl 5-chloro-1-(3-chlorophenyl)-1H-pyrazole-4-carboxylate serves as a crucial intermediate in the synthesis of various pharmaceuticals. Its unique structure allows for the development of new drugs with specific therapeutic targets, contributing to advancements in medicine.
Used in Agrochemical Industry:
In the agrochemical sector, Ethyl 5-chloro-1-(3-chlorophenyl)-1H-pyrazole-4-carboxylate is utilized as an intermediate for the production of pesticides and other crop protection agents. Its incorporation aids in the creation of effective solutions to combat pests and diseases, thereby enhancing agricultural productivity and crop yields.
Used in Research and Development:
Ethyl 5-chloro-1-(3-chlorophenyl)-1H-pyrazole-4-carboxylate is also employed as a subject of research for exploring its biological activities and potential applications. Scientists investigate its interactions with biological systems to uncover new avenues for drug discovery and therapeutic interventions.
Check Digit Verification of cas no
The CAS Registry Mumber 98534-74-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,5,3 and 4 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 98534-74:
(7*9)+(6*8)+(5*5)+(4*3)+(3*4)+(2*7)+(1*4)=178
178 % 10 = 8
So 98534-74-8 is a valid CAS Registry Number.
InChI:InChI=1/C12H10Cl2N2O2/c1-2-18-12(17)10-7-15-16(11(10)14)9-5-3-4-8(13)6-9/h3-7H,2H2,1H3
98534-74-8Relevant academic research and scientific papers
4-carboxy-1-phenyl-5-pyrazolecarboxamides in the production of hybrid cereal grain seed
-
, (2008/06/13)
Pollen formation in cereal grain plants is inhibited by application of a 4-carboxy(or derivative)-1-aryl-5-pyrazolecarboxamide. Production of hybrid seed is facilitated by use of the compounds.
Pollen formation inhibiting 1-phenyl-4-carboxy-5-pyrazolecarboxamides
-
, (2008/06/13)
Pollen formation in cereal grain plants is inhibited by application of a 4-carboxy(or derivative)-1-aryl-5-pyrazolecarboxamide. Production of hybrid seed is facilitated by use of the compounds.
Nonaqueous Diazotation of 5-Amino-1-aryl-1H-pyrazole-4-carboxylate Esters
Beck, James R.,Gajewski, Robert P.,Lynch, Michael P.,Wright, Fred L.
, p. 267 - 270 (2007/10/02)
5-Amino-1-aryl-1H-pyrazole-4-carboxylate esters are converted to the corresponding desamino, chloro, bromo, iodo, and methylthio esters by processes involving nonaqueous diazotation.Diazotizing agents are alkyl nitrites except in the case of chlorine wher
Herbicidal and algicidal 1,5-disubstituted-1H-pyrazole-4-carboxamides
-
, (2008/06/13)
1,5-Disubstituted-1H-pyrazole-4-carboxamide derivatives, useful as herbicides and aquatic algicides.