73955-55-2 Usage
Uses
Used in Pharmaceutical Industry:
4-Pyrimidinecarboxylic acid, 2-methyl-, methyl ester (9CI) is used as a reactant in the preparation of pyrimidine derivatives, which are essential building blocks for the synthesis of various pharmaceutical compounds. These pyrimidine-based compounds have a wide range of applications in the development of drugs targeting different therapeutic areas, such as antiviral, anticancer, and antimalarial agents.
Used in Chemical Research:
In the field of chemical research, 4-Pyrimidinecarboxylic acid, 2-methyl-, methyl ester (9CI) serves as a valuable intermediate for the synthesis of novel pyrimidine-based compounds with potential applications in various industries. Researchers can use 4-Pyrimidinecarboxylicacid,2-methyl-,methylester(9CI) to explore new chemical reactions and develop innovative synthetic routes for the preparation of complex pyrimidine derivatives.
Used in Agrochemical Industry:
4-Pyrimidinecarboxylic acid, 2-methyl-, methyl ester (9CI) can also be utilized in the agrochemical industry for the development of new pesticides and herbicides. Pyrimidine-based compounds have shown potential as effective agents in controlling pests and weeds, making them valuable components in the design of new agrochemical products.
Check Digit Verification of cas no
The CAS Registry Mumber 73955-55-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,9,5 and 5 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 73955-55:
(7*7)+(6*3)+(5*9)+(4*5)+(3*5)+(2*5)+(1*5)=162
162 % 10 = 2
So 73955-55-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H8N2O2/c1-5-8-4-3-6(9-5)7(10)11-2/h3-4H,1-2H3
73955-55-2Relevant academic research and scientific papers
Probing the Scope of the Amidine–1,2,3-triazine Cycloaddition as a Prospective Click Ligation Method
Siegl, Sebastian J.,Vrabel, Milan
supporting information, p. 5081 - 5085 (2018/10/20)
Despite recent achievements in the development of chemical reactions enabling selective modification of complex biomolecules, the demand for fast and efficient methodologies that allow the attachment of various functional groups to these systems is the subject of intense research. Here, we report on the study of the amidine–1,2,3-triazine cycloaddition reaction, which has the potential to address many of the challenges associated with the development of such chemistry. We describe an optimized protocol leading to the in situ formation of free amidine bases, which directly react in the cycloaddition reaction with 1,2,3-triazines. Our kinetic studies reveal the structural features determining the reaction rates. Finally, we show that the amidine–1,2,3-triazine cycloaddition is extraordinarily selective and orthogonal to other popular ligation reactions. The pros and cons of the methodology are presented.
