38373-46-5 Usage
Uses
Used in Pharmaceutical Research:
Methyl 2-MethoxypyriMidine-5-carboxylate is used as a building block for the synthesis of various biologically active molecules, contributing to the development of new drugs. Its unique chemical properties and structural characteristics make it a promising candidate for creating innovative pharmaceutical compounds.
Used in Agrochemical Research:
Similarly, in agrochemical research, Methyl 2-MethoxypyriMidine-5-carboxylate serves as an intermediate in the synthesis of new pesticides. Its role in creating effective and novel agrochemicals is significant, potentially leading to advancements in crop protection and management.
Used in the Production of Fine Chemicals:
Methyl 2-MethoxypyriMidine-5-carboxylate is also utilized as an intermediate in the production of other fine chemicals, highlighting its versatility and importance in the chemical industry.
Safety Note:
Given its applications, Methyl 2-MethoxypyriMidine-5-carboxylate should be handled and used with caution, adhering to proper safety procedures and guidelines to ensure the well-being of individuals and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 38373-46-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,3,7 and 3 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 38373-46:
(7*3)+(6*8)+(5*3)+(4*7)+(3*3)+(2*4)+(1*6)=135
135 % 10 = 5
So 38373-46-5 is a valid CAS Registry Number.
38373-46-5Relevant academic research and scientific papers
A general procedure for the synthesis of 2-substituted pyrimidine-5-carboxylic esters
Zhichkin, Pavel,Fairfax, David J.,Eisenbeis, Shane A.
, p. 720 - 722 (2007/10/03)
A method for the synthesis of 2-substituted pyrimidine-5-carboxylic esters is described. The sodium salt of 3,3-dimethoxy-2-methoxycarbonylpropen-1-ol (3) has been found to react with a variety of amidinium salts to afford the corresponding 2-substituted pyrimidine-5-carboxylic esters.
Reaction of esters of 2-substituted 5-pyrimidinecarboxylic acids with hydrazine hydrate
Tumkevicius,Yakubkene,Vainilavicius
, p. 1334 - 1336 (2007/10/03)
The reaction of methyl esters of 2-substituted 5-pyrimidinecarboxylic acids with hydrazine hydrate at 0-5°C results in the nucleophilic substitution of readily eliminating groups (Cl, CH3O, CH3S) at the position 2 of the pyrimidine r
