CAS 39083-15-3
:5-ethyl-6-methyl-2-thioxo-2,3-dihydropyrimidin-4(1H)-one
Description:
5-Ethyl-6-methyl-2-thioxo-2,3-dihydropyrimidin-4(1H)-one, with the CAS number 39083-15-3, is a heterocyclic compound that belongs to the class of pyrimidinones. This compound features a pyrimidine ring substituted with an ethyl group at the 5-position and a methyl group at the 6-position, along with a thioxo group at the 2-position. The presence of the thioxo group contributes to its reactivity and potential biological activity. Typically, compounds of this nature may exhibit various pharmacological properties, making them of interest in medicinal chemistry. The structural characteristics, including the dihydropyrimidinone framework, suggest potential applications in the development of pharmaceuticals, particularly as enzyme inhibitors or in the synthesis of other biologically active molecules. Additionally, the compound's solubility and stability can vary based on environmental conditions, influencing its practical applications in research and industry. Overall, 5-ethyl-6-methyl-2-thioxo-2,3-dihydropyrimidin-4(1H)-one represents a versatile structure with potential implications in various chemical and biological fields.
Formula:C7H10N2OS
InChI:InChI=1/C7H10N2OS/c1-3-5-4(2)8-7(11)9-6(5)10/h3H2,1-2H3,(H2,8,9,10,11)
SMILES:CCc1c(C)nc(nc1O)S
Synonyms:- 4(3H)-pyrimidinone, 5-ethyl-2-mercapto-6-methyl-
- 4-Pyrimidinol, 5-Ethyl-2-Mercapto-6-Methyl-
- 5-Ethyl-6-methyl-2-sulfanylpyrimidin-4-ol
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 3 products.
5-Ethyl-6-methyl-2-thioxo-2,3-dihydropyrimidin-4(1H)-one
CAS:5-Ethyl-6-methyl-2-thioxo-2,3-dihydropyrimidin-4(1H)-onePurity:98%5-ethyl-2-mercapto-6-methylpyrimidin-4(3H)-one
CAS:Formula:C7H10N2OSPurity:98%Molecular weight:170.235-Ethyl-6-methyl-2-thioxo-2,3-dihydropyrimidin-4(1H)-one
CAS:<p>5-Ethyl-6-methyl-2-thioxo-2,3-dihydropyrimidin-4(1H)-one is a chemical compound containing an iodide group and a nitrogen atom. Iodides can be formed by the iodocyclization of ethyl acetoacetate with ethyl iodide. The resulting 5-ethyl-6-methylpyrimidinecarboxylic acid can be converted to the desired product by treatment with potassium hydroxide in ethanol.</p>Formula:C7H10N2OSPurity:Min. 95%Molecular weight:170.23 g/mol



