5-(Methylsulfanyl)-1,2,4-thiadiazol-3(2H)-one is a heterocyclic compound characterized by the presence of a thiadiazole ring, which consists of two nitrogen atoms and one sulfur atom in a five-membered ring structure. The compound features a methylsulfanyl group, which contributes to its unique chemical properties and potential biological activity. It is typically a solid at room temperature and may exhibit moderate solubility in polar solvents due to the presence of the thiol and carbonyl functional groups. This compound is of interest in various fields, including medicinal chemistry and agrochemicals, due to its potential applications as a bioactive agent. The presence of the thiadiazole moiety is often associated with diverse pharmacological activities, including antimicrobial and antifungal properties. Additionally, the compound's stability and reactivity can be influenced by the substituents on the thiadiazole ring, making it a subject of study for further chemical modifications and applications in drug development.

5-(methylsulfanyl)-1,2,4-thiadiazol-3(2H)-one

56409-41-7: 5-(Methylsulfanyl)-1,2,4-thiadiazol-3(2H)-one is a heterocyclic compound characterized by the presence of a thiadiazole ring, which consists of two nitrogen atoms and one sulfur atom in a five-membered ring structure. The compound features a methylsulfanyl group, which contributes to its unique chemical properties and potential biological activity. It is typically a solid at room temperature and may exhibit moderate solubility in polar solvents due to the presence of the thiol and carbonyl functional groups. This compound is of interest in various fields, including medicinal chemistry and agrochemicals, due to its potential applications as a bioactive agent. The presence of the thiadiazole moiety is often associated with diverse pharmacological activities, including antimicrobial and antifungal properties. Additionally, the compound's stability and reactivity can be influenced by the substituents on the thiadiazole ring, making it a subject of study for further chemical modifications and applications in drug development.

CAS 56409-41-7

5-(methylsulfanyl)-1,2,4-thiadiazol-3(2H)-one

3-Hydroxy-5-methylmercapto-1,2,4-thiadiazole

Ref: 10-F005951