3-Methylthiophene-2-sulfonamide is an organic compound characterized by its thiophene ring structure, which is a five-membered aromatic ring containing sulfur. The presence of a methyl group at the 3-position and a sulfonamide functional group at the 2-position contributes to its unique chemical properties. This compound typically exhibits moderate solubility in polar solvents due to the sulfonamide group, which can engage in hydrogen bonding. It may also display interesting reactivity patterns, particularly in electrophilic substitution reactions, owing to the electron-donating nature of the methyl group and the electron-withdrawing characteristics of the sulfonamide. Additionally, 3-methylthiophene-2-sulfonamide may have applications in pharmaceuticals or agrochemicals, given the biological activity often associated with thiophene derivatives. Its molecular structure allows for potential interactions with biological targets, making it a subject of interest in medicinal chemistry. Safety and handling precautions should be observed, as with any chemical substance, to mitigate risks associated with its use.

3-methylthiophene-2-sulfonamide

81417-51-8: 3-Methylthiophene-2-sulfonamide is an organic compound characterized by its thiophene ring structure, which is a five-membered aromatic ring containing sulfur. The presence of a methyl group at the 3-position and a sulfonamide functional group at the 2-position contributes to its unique chemical properties. This compound typically exhibits moderate solubility in polar solvents due to the sulfonamide group, which can engage in hydrogen bonding. It may also display interesting reactivity patterns, particularly in electrophilic substitution reactions, owing to the electron-donating nature of the methyl group and the electron-withdrawing characteristics of the sulfonamide. Additionally, 3-methylthiophene-2-sulfonamide may have applications in pharmaceuticals or agrochemicals, given the biological activity often associated with thiophene derivatives. Its molecular structure allows for potential interactions with biological targets, making it a subject of interest in medicinal chemistry. Safety and handling precautions should be observed, as with any chemical substance, to mitigate risks associated with its use.

CAS 81417-51-8

3-methylthiophene-2-sulfonamide

3-methylthiophene-2-sulfonamide

Ref: 10-F515379

3-Methylthiophene-2-sulfonamide

Ref: 3D-GDA41751