5933-30-2 Usage
General Description
6-Methylpyridine-2-thioamide is a chemical compound with the molecular formula C7H8N2S. It is a heterocyclic aromatic ring with a sulfur atom in the 2-position and a methyl group at the 6-position. 6-methylpyridine-2-thioamide is commonly used as a building block in the synthesis of various organic compounds. It has been identified as a component in the structure of certain pharmaceuticals, pesticides, and catalysts. In addition, 6-Methylpyridine-2-thioamide possesses potential biological activities and has shown promise in various medicinal and agricultural applications. Due to its diverse applications, this compound is of interest in the fields of chemistry, biochemistry, and pharmaceutical research.
Check Digit Verification of cas no
The CAS Registry Mumber 5933-30-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,3 and 3 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5933-30:
(6*5)+(5*9)+(4*3)+(3*3)+(2*3)+(1*0)=102
102 % 10 = 2
So 5933-30-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H8N2S/c1-5-3-2-4-6(9-5)7(8)10/h2-4H,1H3,(H2,8,10)
5933-30-2Relevant articles and documents
A efficient protocol for the synthesis of thioamides in [DBUH][OAc] at room temperature
Cao, Xian-Ting,Qiao, Li,Zheng, Hui,Yang, Hui-Yong,Zhang, Peng-Fei
, p. 170 - 175 (2018/01/17)
A novel, simple and eco-friendly method to synthesize thioamides from aryl nitriles and sodium sulfide (Na2S·9H2O) catalyzed by 1,8-diazabicyclo[5,4,0]undec-7-enium acetate ([DBUH][OAc]) ionic liquid (IL) at room temperature was developed in this paper. In this reaction, readily available inorganic salt (Na2S·9H2O) serves as the sulfur source, and various functional groups of aryl nitriles were well tolerated at room temperature. In addition, the products were easily separated from the IL which could be reused at least five times without considerable loss of its activity and applied in the green, concise synthesis of ethionamide.
