38275-42-2 Usage
Description
2-METHYLSULFANYL-5-CHLOROPYRIMIDINE, with the molecular formula C5H5ClN2S, is a pyrimidine derivative characterized by the presence of a methylthio group and a chlorine atom attached to the pyrimidine ring. This chemical compound is recognized for its versatile reactivity and potential biological activity, making it a valuable building block in the creation of novel compounds for various applications.
Uses
Used in Pharmaceutical Synthesis:
2-METHYLSULFANYL-5-CHLOROPYRIMIDINE is used as a key intermediate in the synthesis of pharmaceuticals for its potential biological activity and versatile reactivity. It contributes to the development of new drugs with therapeutic benefits.
Used in Agrochemical Production:
In the agrochemical industry, 2-METHYLSULFANYL-5-CHLOROPYRIMIDINE serves as an essential intermediate, facilitating the production of compounds with pesticidal or herbicidal properties, thereby enhancing crop protection and yield.
Used in Organic Compound Production:
2-METHYLSULFANYL-5-CHLOROPYRIMIDINE is utilized as a valuable building block in the creation of other organic compounds, expanding its applications across different chemical and material science fields. Its unique structural features allow for the synthesis of a wide range of novel compounds with diverse properties and potential uses.
Check Digit Verification of cas no
The CAS Registry Mumber 38275-42-2 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, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 38275-42:
(7*3)+(6*8)+(5*2)+(4*7)+(3*5)+(2*4)+(1*2)=132
132 % 10 = 2
So 38275-42-2 is a valid CAS Registry Number.
38275-42-2Relevant articles and documents
Decarboxylation in the synthesis of 4-alkyl-, 4-alkenyl- and 4-acylpyrimidines
Herstad, Gunnar,Benneche, Tore
, p. 219 - 224 (2007/10/03)
Decarboxylation of allylic esters of 4-carboxypyrimidines in toluene at 111°C in the presence of a Pd(0) catalyst, gives a mixture of a 4-alkenylpyrimidine and a pyrimidine unsubstituted in the 4-position. If the decarboxylation is carried out in the presence of benzaldehyde, then benzaldehyde is added to the 4-position. Decarboxylation of 4-carboxypyrimidines in the presence of different electrophiles, results in incorporation of the electrophile into the 4-position together with a pyrimidine unsubstituted in the 4-position. Use of microwave irradiation enhances the rate of the decarboxylations.
