2-(2-Thienylsulfonyl)ethanethioamide is a chemical compound characterized by its thienyl group, which is a five-membered aromatic ring containing sulfur. This compound features a sulfonyl group, which contributes to its reactivity and solubility in various solvents. The presence of the thioamide functional group indicates that it can participate in various chemical reactions, including nucleophilic substitutions and condensation reactions. Typically, compounds like this may exhibit biological activity, making them of interest in medicinal chemistry and drug development. The molecular structure suggests potential interactions with biological targets, which could lead to pharmacological effects. Additionally, the compound's properties, such as melting point, boiling point, and solubility, would depend on its molecular interactions and the presence of functional groups. Safety data and handling precautions are essential when working with this compound, as with many thienyl and sulfonyl derivatives, due to potential toxicity or reactivity. Overall, 2-(2-thienylsulfonyl)ethanethioamide represents a unique structure with potential applications in various fields of chemistry and biology.

2-(2-thienylsulfonyl)ethanethioamide

175202-34-3: 2-(2-Thienylsulfonyl)ethanethioamide is a chemical compound characterized by its thienyl group, which is a five-membered aromatic ring containing sulfur. This compound features a sulfonyl group, which contributes to its reactivity and solubility in various solvents. The presence of the thioamide functional group indicates that it can participate in various chemical reactions, including nucleophilic substitutions and condensation reactions. Typically, compounds like this may exhibit biological activity, making them of interest in medicinal chemistry and drug development. The molecular structure suggests potential interactions with biological targets, which could lead to pharmacological effects. Additionally, the compound's properties, such as melting point, boiling point, and solubility, would depend on its molecular interactions and the presence of functional groups. Safety data and handling precautions are essential when working with this compound, as with many thienyl and sulfonyl derivatives, due to potential toxicity or reactivity. Overall, 2-(2-thienylsulfonyl)ethanethioamide represents a unique structure with potential applications in various fields of chemistry and biology.

CAS 175202-34-3

2-(2-thienylsulfonyl)ethanethioamide

2-(thiophene-2-sulfonyl)ethanethioamide

Ref: IN-DA0020GF

2-[(Thien-2-yl)sulphonyl]thioacetamide

Ref: 54-OR25256

2-(Thiophen-2-ylsulfonyl)ethanethioamide

Ref: 10-F556699