915376-16-8 Usage
Description
Methyl 4-methyl-2-(trifluoromethyl)pyrimidine-5-carboxylate is a pyrimidine derivative with the molecular formula C9H8F3N3O2. It features a methyl ester functional group, a trifluoromethyl group, and a carboxylate group, making it a versatile compound in the pharmaceutical industry.
Uses
Used in Pharmaceutical Industry:
Methyl 4-methyl-2-(trifluoromethyl)pyrimidine-5-carboxylate serves as a building block for the synthesis of various drugs and medicinal compounds, contributing to the development of new treatments and therapies.
Used in Research and Development:
Due to its unique structural properties and potential pharmacological activities, this compound is utilized in the research and development of new pharmaceutical products, aiding in the discovery and innovation of novel medications.
Used as a Reference Standard:
Methyl 4-methyl-2-(trifluoromethyl)pyrimidine-5-carboxylate is employed as a reference standard in analytical testing and quality control procedures in chemical and pharmaceutical laboratories, ensuring the accuracy and reliability of testing results.
Check Digit Verification of cas no
The CAS Registry Mumber 915376-16-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,5,3,7 and 6 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 915376-16:
(8*9)+(7*1)+(6*5)+(5*3)+(4*7)+(3*6)+(2*1)+(1*6)=178
178 % 10 = 8
So 915376-16-8 is a valid CAS Registry Number.
915376-16-8Relevant articles and documents
Insecticidal anthranilic diamides: A new class of potent ryanodine receptor activators
Lahm, George P.,Selby, Thomas P.,Freudenberger, John H.,Stevenson, Thomas M.,Myers, Brian J.,Seburyamo, Gilles,Smith, Ben K.,Flexner, Lindsey,Clark, Christopher E.,Cordova, Daniel
, p. 4898 - 4906 (2007/10/03)
A novel class of anthranilic diamides has been discovered with exceptional insecticidal activity on a range of Lepidoptera. These compounds have been found to exhibit their action by release of intracellular Ca2+ stores mediated by the ryanodine receptor. The discovery, synthesis, structure-activity, and biological results are presented.
