N-3-Thienylacetamide is an organic compound characterized by the presence of a thienyl group, which is a five-membered aromatic ring containing sulfur, attached to an acetamide functional group. This compound typically exhibits properties associated with both aromatic and amide functionalities, including potential solubility in polar solvents due to the amide group and some degree of stability due to the aromatic thienyl structure. The thienyl moiety can contribute to unique electronic properties, making N-3-Thienylacetamide of interest in various chemical applications, including pharmaceuticals and agrochemicals. Its molecular structure suggests it may participate in hydrogen bonding due to the amide group, influencing its reactivity and interactions with other molecules. Additionally, compounds like N-3-Thienylacetamide may exhibit biological activity, which can be explored in medicinal chemistry. Overall, the characteristics of this compound make it a subject of interest for further research in both synthetic and applied chemistry contexts.

N-3-Thienylacetamide

42602-67-5: 3-(Acetylamino)thiophene, 3-Acetamidothiophene, N-3-Thienylacetamide, Thiophene, 3-acetamido-, Acetamide, N-3-thienyl-

N-(Thiophen-3-yl)acetamide

N-(3-Thienyl)acetamide is an aromatic aldehyde that is used in the synthesis of carbamates. It has been shown to be brominated, acetylated, and aminated. N-(3-Thienyl)acetamide can undergo dehydrogenation and heterocyclic amine formation during cooking. It also has electrophilic properties, which allow it to react with nucleophiles such as amines or thiols to form diazonium salts. This compound is a substrate for transamination and dihydropyridines.

CAS 42602-67-5: N-3-Thienylacetamide

N-(Thiophen-3-yl)acetamide

Ref: 10-F446292

N-(3-Thienyl)acetamide

Ref: 3D-SBA60267

N-(Thiophen-3-yl)acetamide

Ref: IN-DA003SB9

N-3-Thienylacetamide

Ref: 54-OR55684