1H-Indole-6-carbothioamide is an organic compound characterized by its indole structure, which is a bicyclic compound consisting of a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring. The presence of a carbothioamide functional group at the 6-position of the indole ring introduces a thiocarbonyl moiety, which can influence the compound's reactivity and biological activity. This compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. Its unique structure allows for potential interactions with biological targets, making it of interest in medicinal chemistry and drug development. The compound may also exhibit properties such as antimicrobial or anticancer activity, although specific biological effects would depend on further empirical studies. Additionally, its synthesis may involve standard organic reactions, including amide formation and thioketone chemistry. As with many indole derivatives, 1H-Indole-6-carbothioamide may serve as a scaffold for further chemical modifications to enhance its pharmacological properties.

1H-Indole-6-carbothioamide

885272-19-5: 1H-Indole-6-carbothioamide is an organic compound characterized by its indole structure, which is a bicyclic compound consisting of a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring. The presence of a carbothioamide functional group at the 6-position of the indole ring introduces a thiocarbonyl moiety, which can influence the compound's reactivity and biological activity. This compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. Its unique structure allows for potential interactions with biological targets, making it of interest in medicinal chemistry and drug development. The compound may also exhibit properties such as antimicrobial or anticancer activity, although specific biological effects would depend on further empirical studies. Additionally, its synthesis may involve standard organic reactions, including amide formation and thioketone chemistry. As with many indole derivatives, 1H-Indole-6-carbothioamide may serve as a scaffold for further chemical modifications to enhance its pharmacological properties.

CAS 885272-19-5

1H-Indole-6-carbothioamide

1H-Indole-6-carbothioamide

Ref: IN-DA0046XM