1,2,4-Oxadiazole-3-carbothioamide is a heterocyclic compound characterized by the presence of an oxadiazole ring, which consists of two nitrogen atoms and three carbon atoms in a five-membered ring structure. This compound features a carbothioamide functional group, which includes a thiocarbonyl (C=S) moiety attached to an amine (NH2) group. The presence of these functional groups imparts unique chemical properties, such as potential reactivity in nucleophilic substitution and the ability to form hydrogen bonds. 1,2,4-Oxadiazole derivatives are often studied for their biological activities, including antimicrobial and antifungal properties, making them of interest in medicinal chemistry. The compound is typically a solid at room temperature and may exhibit moderate solubility in polar solvents. Its synthesis often involves the reaction of appropriate precursors under controlled conditions. As with many heterocycles, the stability and reactivity of 1,2,4-oxadiazole-3-carbothioamide can be influenced by substituents on the ring and the carbothioamide group, leading to a diverse range of potential applications in pharmaceuticals and agrochemicals.

1,2,4-oxadiazole-3-carbothioamide

39512-80-6: 1,2,4-Oxadiazole-3-carbothioamide is a heterocyclic compound characterized by the presence of an oxadiazole ring, which consists of two nitrogen atoms and three carbon atoms in a five-membered ring structure. This compound features a carbothioamide functional group, which includes a thiocarbonyl (C=S) moiety attached to an amine (NH2) group. The presence of these functional groups imparts unique chemical properties, such as potential reactivity in nucleophilic substitution and the ability to form hydrogen bonds. 1,2,4-Oxadiazole derivatives are often studied for their biological activities, including antimicrobial and antifungal properties, making them of interest in medicinal chemistry. The compound is typically a solid at room temperature and may exhibit moderate solubility in polar solvents. Its synthesis often involves the reaction of appropriate precursors under controlled conditions. As with many heterocycles, the stability and reactivity of 1,2,4-oxadiazole-3-carbothioamide can be influenced by substituents on the ring and the carbothioamide group, leading to a diverse range of potential applications in pharmaceuticals and agrochemicals.

CAS 39512-80-6

1,2,4-oxadiazole-3-carbothioamide

1,2,4-Oxadiazole-3-carbothioamide

Ref: IN-DA00BZH1

1,2,4-Oxadiazole-3-carbothioamide

Ref: 10-F068778

1,2,4-Oxadiazole-3-carbothioamide

Ref: 3D-PBA51280