149771-12-0 Usage
Uses
Used in Pharmaceutical Industry:
Ethyl 2-(methylsulfanyl)-4-(trifluoromethyl)pyrimidine-5-carboxylate is used as a pharmaceutical intermediate for the synthesis of various therapeutic agents. Its unique structure and functional groups contribute to the development of new drugs with potential applications in treating various diseases.
Used in Agrochemical Industry:
In the agrochemical industry, ethyl 2-(methylsulfanyl)-4-(trifluoromethyl)pyrimidine-5-carboxylate is used as a precursor in the synthesis of agrochemicals, such as pesticides and herbicides. Its reactivity and functional groups can be utilized to create compounds with specific properties to control pests and weeds in agriculture.
Used in Material Science:
Ethyl 2-(methylsulfanyl)-4-(trifluoromethyl)pyrimidine-5-carboxylate is used as a building block in the development of new materials with unique properties. Its potential reactivity and functional groups can be exploited to create materials with specific characteristics for various applications in material science.
Used in Organic Synthesis:
As a versatile organic compound, ethyl 2-(methylsulfanyl)-4-(trifluoromethyl)pyrimidine-5-carboxylate is used as a starting material in the synthesis of more complex organic molecules. Its unique structure and functional groups make it a valuable component in the creation of new organic compounds for research and industrial applications.
Check Digit Verification of cas no
The CAS Registry Mumber 149771-12-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,9,7,7 and 1 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 149771-12:
(8*1)+(7*4)+(6*9)+(5*7)+(4*7)+(3*1)+(2*1)+(1*2)=160
160 % 10 = 0
So 149771-12-0 is a valid CAS Registry Number.
149771-12-0Relevant academic research and scientific papers
Synthesis, antiviral (HSV-1) and antimycotic activities of ethyl or methyl 2,4-disubstituted 5-pyrimidinecarboxylates, 2,4-disubstituted 5-pyrimidinecarboxylic acids and 2,4-disubstituted pyrimidines
Sansebastiano,Mosti,Menozzi,Schenone,Muratore,Petta,Debbia,Pesce Schito,Schito
, p. 335 - 355 (2007/10/02)
The synthesis of ethyl or methyl 4-substituted or unsubstituted 2-methylthio-5-pyrimidinecarboxylates 3 a-i and 8 o mainly by reaction of ethyl or methyl 2-dimethylaminomethylene-3-oxoalkanoates with 2-methylisothiourea is described. Also some ethyl 2-sub
