5-(Methylsulfanyl)-1,2,4-thiadiazol-3-amine is a heterocyclic compound characterized by the presence of a thiadiazole ring, which contains both sulfur and nitrogen atoms. This compound features a methylsulfanyl group (-S-CH3) attached to the thiadiazole structure, contributing to its unique chemical properties. The presence of an amino group (-NH2) at the 3-position of the thiadiazole enhances its potential for reactivity, particularly in nucleophilic substitution reactions. The compound is typically a solid at room temperature and may exhibit moderate solubility in polar solvents due to the presence of the amino group. Its structure suggests potential applications in pharmaceuticals, agrochemicals, or as a building block in organic synthesis. The compound's reactivity can be influenced by the electron-donating nature of the methylsulfanyl group and the electron-withdrawing characteristics of the thiadiazole ring. Overall, 5-(methylsulfanyl)-1,2,4-thiadiazol-3-amine is of interest for its potential biological activity and utility in various chemical applications.

5-(methylsulfanyl)-1,2,4-thiadiazol-3-amine

60093-10-9: 5-(Methylsulfanyl)-1,2,4-thiadiazol-3-amine is a heterocyclic compound characterized by the presence of a thiadiazole ring, which contains both sulfur and nitrogen atoms. This compound features a methylsulfanyl group (-S-CH3) attached to the thiadiazole structure, contributing to its unique chemical properties. The presence of an amino group (-NH2) at the 3-position of the thiadiazole enhances its potential for reactivity, particularly in nucleophilic substitution reactions. The compound is typically a solid at room temperature and may exhibit moderate solubility in polar solvents due to the presence of the amino group. Its structure suggests potential applications in pharmaceuticals, agrochemicals, or as a building block in organic synthesis. The compound's reactivity can be influenced by the electron-donating nature of the methylsulfanyl group and the electron-withdrawing characteristics of the thiadiazole ring. Overall, 5-(methylsulfanyl)-1,2,4-thiadiazol-3-amine is of interest for its potential biological activity and utility in various chemical applications.

CAS 60093-10-9

5-(methylsulfanyl)-1,2,4-thiadiazol-3-amine

3-Amino-5-methylthio-1,2,4-thiadiazole

Ref: 54-OR322242

3-Amino-5-methylthio-1,2,4-thiadiazole

Ref: 10-F009668