17573-79-4 Usage
Uses
Used in Pharmaceutical Development:
Pyrimidine, 2,4,5-trifluoro(8CI,9CI) is utilized as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique structure and properties make it a valuable component in the development of new drugs, particularly those targeting specific biological pathways or exhibiting enhanced pharmacokinetic profiles.
Used in Agrochemical Production:
This 2,4,5-trifluoropyrimidine is also employed as a building block in the production of agrochemicals. Its chemical properties allow for the creation of compounds with improved efficacy and selectivity in agricultural applications, contributing to more effective pest control and crop protection.
Used in Materials Science:
The 2,4,5-trifluoropyrimidine structure may have potential applications in the field of materials science. Its unique properties could be leveraged to develop new materials with specific characteristics, such as improved stability, reactivity, or selectivity, which can be beneficial in various industrial processes.
Used in Organic Synthesis:
Pyrimidine, 2,4,5-trifluoro(8CI,9CI) serves as a versatile building block in organic synthesis, enabling the creation of a wide range of fluorinated compounds with diverse applications. Its presence in the synthesis process can significantly influence the final product's properties, making it an essential component in the development of new organic compounds for various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 17573-79-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,5,7 and 3 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 17573-79:
(7*1)+(6*7)+(5*5)+(4*7)+(3*3)+(2*7)+(1*9)=134
134 % 10 = 4
So 17573-79-4 is a valid CAS Registry Number.
17573-79-4Relevant academic research and scientific papers
Baasner, B.,Klauke, E.
, p. 417 - 430 (1989)
Starting from tetrafluoropyrimidine (1), selective fluorine/chlorine exchange reactions and selective hydrogenolysis of the chlorine substituents are described.Combination of these methods, together with a subsequent hydrolysis reaction, provides a new route to the synthesis of 5-fluorouracil via 4,6-dichloro-2,5-difluoropyrimidine and 4-chloro-2,5-difluoropyrimidine.
