4-(1,3-Dithiolan-2-yl)benzene-1-carbothioamide is a chemical compound characterized by its unique structure, which includes a benzene ring substituted with a dithiolan moiety and a carbothioamide functional group. The presence of the dithiolan ring contributes to its potential reactivity and stability, while the carbothioamide group introduces a thiolamide functionality that can participate in various chemical reactions, such as nucleophilic attacks or coordination with metal ions. This compound may exhibit interesting properties, including potential biological activity, due to the presence of sulfur atoms, which can influence its interaction with biological systems. Additionally, the compound's solubility, melting point, and other physical properties would depend on its molecular interactions and the presence of functional groups. As with many sulfur-containing compounds, it may also exhibit distinct odor characteristics. Overall, 4-(1,3-dithiolan-2-yl)benzene-1-carbothioamide is of interest in synthetic chemistry and may have applications in materials science or medicinal chemistry, pending further research into its properties and potential uses.

4-(1,3-dithiolan-2-yl)benzene-1-carbothioamide

175204-52-1: 4-(1,3-Dithiolan-2-yl)benzene-1-carbothioamide is a chemical compound characterized by its unique structure, which includes a benzene ring substituted with a dithiolan moiety and a carbothioamide functional group. The presence of the dithiolan ring contributes to its potential reactivity and stability, while the carbothioamide group introduces a thiolamide functionality that can participate in various chemical reactions, such as nucleophilic attacks or coordination with metal ions. This compound may exhibit interesting properties, including potential biological activity, due to the presence of sulfur atoms, which can influence its interaction with biological systems. Additionally, the compound's solubility, melting point, and other physical properties would depend on its molecular interactions and the presence of functional groups. As with many sulfur-containing compounds, it may also exhibit distinct odor characteristics. Overall, 4-(1,3-dithiolan-2-yl)benzene-1-carbothioamide is of interest in synthetic chemistry and may have applications in materials science or medicinal chemistry, pending further research into its properties and potential uses.

CAS 175204-52-1

4-(1,3-dithiolan-2-yl)benzene-1-carbothioamide

Benzenecarbothioamide, 4-(1,3-dithiolan-2-yl)-

Ref: IN-DA0020M0

4-(1,3-dithiolan-2-yl)benzene-1-carbothioamide

Ref: 54-OR27298