38275-34-2 Usage
General Description
5-Chloro-2-(methylsulfonyl)pyrimidine-4-carboxylic acid is a chemical compound categorized under the group of pyrimidines and their derivatives. The name reflects its structure, which includes a chlorine atom, a methylsulfonyl group, and a carboxylic acid group attached to the pyrimidine category. 5-CHLORO-2-(METHYLSULFONYL)PYRIMIDINE-4-CARBOXYLIC ACID is used in various chemical reactions as an intermediate to synthesize other more complex chemicals. Its detailed physical properties like melting point, boiling point, density, solubility, and stability, etc., differ based on the conditions they are subject to. 5-CHLORO-2-(METHYLSULFONYL)PYRIMIDINE-4-CARBOXYLIC ACID requires appropriate safety measures during handling and storage particularly due to the reactivity of the pyrimidine moiety and corrosiveness of the carboxylic acid group.
Check Digit Verification of cas no
The CAS Registry Mumber 38275-34-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,2,7 and 5 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 38275-34:
(7*3)+(6*8)+(5*2)+(4*7)+(3*5)+(2*3)+(1*4)=132
132 % 10 = 2
So 38275-34-2 is a valid CAS Registry Number.
38275-34-2Relevant articles and documents
Efficient synthesis of a new pyrimidine derivative
Liang, Yong-Min,Luo, Sheng-Jun,Zhang, Zhao-Xin,Ma, Yong-Xiang
, p. 153 - 157 (2002)
A ready preparation for a new pyrimidine derivative, 2-aminomethyl-5-chloropyrimidine, from s-methylthiouronium sulphate and mucochloric acid is reported.
General and facial synthesis of 2-amino-5-halogenpyrimidine-4-carboxylic acids and their derivatives
Blyumin, Evgeniy V.,Neunhoeffer, Hans,Volovenko, Yulian V.
, p. 2231 - 2241 (2008/02/07)
A facile synthetic approach to 2-amino-5-halogen-pyrimidine-4-carboxylic acids from 5-halogen-2-methylsulfonylpyrimidine-4-carboxylic acid by nucleophilic displacement of the methylsulfonyl group with primary and secondary aliphatic amines has been develo
