14001-64-0 Usage
Description
4,6-Dimethyl-2-methylmercapyrimidine is an organic compound characterized by its white solid appearance. It is a heterocyclic compound with a pyrimidine ring structure, featuring two methyl groups at the 4 and 6 positions and a methylmercapto group at the 2 position. 4,6-Dimethyl-2-methylmercapyrimidine is known for its potential applications in various chemical and pharmaceutical processes due to its unique structural properties.
Uses
Used in Chemical Synthesis:
4,6-Dimethyl-2-methylmercapyrimidine is used as a reactant for the synthesis of substituted heterocycles. Its unique structure allows it to participate in nickel-catalyzed cross-coupling reactions, which are essential for creating a wide range of complex and functionalized heterocyclic compounds. These synthesized heterocycles can be further utilized in various applications, such as pharmaceuticals, agrochemicals, and advanced materials.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4,6-Dimethyl-2-methylmercapyrimidine can be used as a building block for the development of new drugs. Its structural properties make it a valuable candidate for the synthesis of bioactive molecules with potential therapeutic applications. The compound can be further modified and optimized to target specific biological pathways or receptors, leading to the discovery of novel therapeutic agents.
Used in Material Science:
4,6-Dimethyl-2-methylmercapyrimidine can also be employed in the development of advanced materials due to its unique chemical and structural properties. Its potential use in material science includes the creation of new polymers, dyes, or sensors with specific properties tailored for various applications, such as electronics, energy storage, or environmental monitoring.
Check Digit Verification of cas no
The CAS Registry Mumber 14001-64-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,0,0 and 1 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 14001-64:
(7*1)+(6*4)+(5*0)+(4*0)+(3*1)+(2*6)+(1*4)=50
50 % 10 = 0
So 14001-64-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H10N2S/c1-5-4-6(2)9-7(8-5)10-3/h4H,1-3H3
14001-64-0Relevant articles and documents
Regioselectivity in the amination of methylsulfanyl-substituted azines with O-mesitylenesulfonylhydroxylamine
Borodkin,Vorob'Ev,Shakirov,Shubin
, p. 911 - 916 (2010)
Reactions of O-mesitylenesulfonylhydroxylamine with 2-(methylsulfanyl) pyrazine, 2-(methylsulfanyl) pyrimidine, and 3,5-dimethyl-2-(methylsulfanyl) pyrimidines involve both sulfur and nitrogen atoms. The amination products at the sulfur atom prevail in th
SH-methylation of SH-containing heterocycles with dimethyl carbonate via phase-transfer catalytic reaction
Xie, Jian-Gang,Quan, Jing,Li, Shu-Bai,Zheng, Yan,Zhu, Li-Min
experimental part, p. 871 - 878 (2011/04/22)
A reaction of SH-containing heterocycles with dimethyl carbonate (DMC) in the presence of K2CO3 and tetrabutylammonium bromide (Bu4NBr) gave heteroaryl methyl thioethers in 44-93% yields. The reaction was carried out under mild conditions. This method provided a useful synthetic method for preparation of various heteroaryl methyl thioethers without the use of toxic methylic halides or dimethyl sulfate.
An easy and fast ultrasonic selective S-alkylation of hetaryl thiols at room temperature
Deligeorgiev, Todor,Kaloyanova, Stefka,Lesev, Nedyalko,Vaquero, Juan J.
experimental part, p. 783 - 788 (2011/10/09)
A series of 2-alkylthio derivatives of hetaryl thiols were synthesized by selective S-alkylation with alkyl halides (bromides and iodides) with ultrasonic irradiation at room temperature. The reaction was found to be generally applicable to hetaryl thiol derivatives with different substituents in the aromatic nucleus and various alkyl halides. The reaction gives high to excellent yields of products with high purity.
