Thiophene-3-carbothioamide is an organic compound characterized by the presence of a thiophene ring, which is a five-membered aromatic heterocycle containing sulfur. The compound features a carbothioamide functional group, which consists of a carbonyl group (C=O) bonded to a sulfur atom (S) and an amine (NH2) group. This structure imparts unique chemical properties, including potential reactivity in nucleophilic substitution and condensation reactions. Thiophene derivatives are known for their applications in organic electronics, pharmaceuticals, and as intermediates in synthetic chemistry. The presence of the thiophene ring contributes to the compound's aromaticity, enhancing its stability and influencing its electronic properties. Additionally, the carbothioamide group can participate in hydrogen bonding and may exhibit varying solubility in different solvents, depending on the substituents and the overall molecular structure. Overall, thiophene-3-carbothioamide is of interest in various fields, including materials science and medicinal chemistry, due to its versatile reactivity and potential applications.

thiophene-3-carbothioamide

24044-76-6: Thiophene-3-carbothioamide is an organic compound characterized by the presence of a thiophene ring, which is a five-membered aromatic heterocycle containing sulfur. The compound features a carbothioamide functional group, which consists of a carbonyl group (C=O) bonded to a sulfur atom (S) and an amine (NH2) group. This structure imparts unique chemical properties, including potential reactivity in nucleophilic substitution and condensation reactions. Thiophene derivatives are known for their applications in organic electronics, pharmaceuticals, and as intermediates in synthetic chemistry. The presence of the thiophene ring contributes to the compound's aromaticity, enhancing its stability and influencing its electronic properties. Additionally, the carbothioamide group can participate in hydrogen bonding and may exhibit varying solubility in different solvents, depending on the substituents and the overall molecular structure. Overall, thiophene-3-carbothioamide is of interest in various fields, including materials science and medicinal chemistry, due to its versatile reactivity and potential applications.

CAS 24044-76-6

thiophene-3-carbothioamide

THIOPHENE-3-THIOAMIDE

Ref: IN-DA00BE1Q

Thiophene-3-thiocarboxamide

Ref: 54-OR25930

Thiophene-3-carbothioic acid amide

Ref: 10-F021347