224313-74-0 Usage
Uses
Used in Pharmaceutical Industry:
Methyl 2-hydroxy-4-oxo-4H-pyrido<1,2-a>pyrimidine-3-carboxylate is utilized as an intermediate in the synthesis of pharmaceuticals. Its unique structure and potential medicinal properties make it a valuable component in the development of new drugs.
Used in Agrochemical Industry:
methyl 2-hydroxy-4-oxo-4H-pyrido<1,2-a>pyrimidine-3-carboxylate is also used as an intermediate in the synthesis of agrochemicals, contributing to the development of new products for agricultural applications.
Used in Medicinal Research:
Methyl 2-hydroxy-4-oxo-4H-pyrido<1,2-a>pyrimidine-3-carboxylate is under investigation for its potential anti-inflammatory and antifungal properties, indicating its potential use in the treatment of various medical conditions.
Overall, methyl 2-hydroxy-4-oxo-4H-pyrido<1,2-a>pyrimidine-3-carboxylate holds promise for various applications within the pharmaceutical and agricultural industries, as well as in medicinal research.
Check Digit Verification of cas no
The CAS Registry Mumber 224313-74-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,4,3,1 and 3 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 224313-74:
(8*2)+(7*2)+(6*4)+(5*3)+(4*1)+(3*3)+(2*7)+(1*4)=100
100 % 10 = 0
So 224313-74-0 is a valid CAS Registry Number.
224313-74-0Relevant academic research and scientific papers
Methanetricarboxylates as key reagents for the simple preparation of heteroarylcarboxamides with potential biological activity. Part 2 [1]. Reaction of methanetricarboxylates with 2-aminopyridine, 2-aminopyrimidine, 2-aminothiazole and 2-aminobenzothiazole
Kutyrev, Alexander,Kappe, Thomas
, p. 237 - 240 (2007/10/03)
The reaction of methanetricarboxylates 1a,b with 2-aminopyridine, 2- aminopyrimidine, 2-aminothiazole as well as 2-aminobenzothiazole yields corresponding heteroarylcarboxylic acid esters 2a,b, 5, 8, 11a,b. These heterocyclic esters were used as a starting material by the reaction with primary amines to obtaining a number of heteroarylcarboxylic amides 4a-j, 6, 10a,b, 13a-g bearing various substituents on the carboxamide group.
