85290-76-2 Usage
Uses
Used in Pharmaceutical Synthesis:
Ethyl 1,3-dimethyl-1H-pyrazole-4-carboxylate is used as an intermediate in the synthesis of pharmaceuticals for its ability to contribute to the formation of complex molecular structures that can exhibit therapeutic properties.
Used in Agrochemical Production:
In the agrochemical industry, Ethyl 1,3-dimethyl-1H-pyrazole-4-carboxylate is utilized as an intermediate in the development of compounds that can be applied in crop protection and pest management, leveraging its chemical reactivity to create effective agents.
Used in Medicinal Chemistry Research:
Ethyl 1,3-dimethyl-1H-pyrazole-4-carboxylate is employed as a research compound in medicinal chemistry, where its structure and reactivity are explored for potential applications in drug discovery and the design of novel therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 85290-76-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,2,9 and 0 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 85290-76:
(7*8)+(6*5)+(5*2)+(4*9)+(3*0)+(2*7)+(1*6)=152
152 % 10 = 2
So 85290-76-2 is a valid CAS Registry Number.
85290-76-2Relevant academic research and scientific papers
Process for the preparation of derivatives of 1-substituted-3-fluoroalkyl-pyrazole-4-carboxylic acid in the presence of ammonium salt
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Paragraph 0049; 0050, (2014/02/15)
A process for the manufacture of a compound of the general formula (I) wherein - Y is H, F, an alkyl group, a cycloalkyl group, an aralkyl group or an aryl group, - R1 is H or an organic residue, - R2 is H or an organic residue ; which comprises submitting a compound of formula (II) wherein Y is as defined above, R1, is H or an organic residue, R2, is H or an organic residue, X is Cl, Br, I, CN, sulphate or sulphonate ; to a reduction reaction in the presence of an ammonium salt.
A one-pot process for the regioselective synthesis of 1,3,4-trisubstituted-1H-pyrazoles
Raw, Steven A.,Turner, Andrew T.
experimental part, p. 696 - 699 (2011/02/27)
This Letter reports a facile and regioselective one-pot synthesis of 1,3,4-trisubstituted-1H-pyrazoles. It comprises a three-step telescoped sequence, which has been utilised in the production of a variety of differentially substituted pyrazoles.
