3-Formylthiophene-2-carboxylic acid is an organic compound characterized by its thiophene ring, which is a five-membered aromatic heterocycle containing sulfur. This compound features both an aldehyde group (-CHO) and a carboxylic acid group (-COOH) attached to the thiophene ring, specifically at the 3 and 2 positions, respectively. The presence of these functional groups contributes to its reactivity and potential applications in organic synthesis and materials science. It is typically a solid at room temperature and may exhibit solubility in polar solvents due to the carboxylic acid group. The compound can participate in various chemical reactions, including condensation and esterification, making it useful in the synthesis of more complex molecules. Additionally, its unique structure allows for potential applications in the development of pharmaceuticals, agrochemicals, and as a building block in organic electronics. As with many thiophene derivatives, it may also exhibit interesting electronic properties, which can be exploited in various applications.

3-formylthiophene-2-carboxylic acid

19991-68-5: 3-Formylthiophene-2-carboxylic acid is an organic compound characterized by its thiophene ring, which is a five-membered aromatic heterocycle containing sulfur. This compound features both an aldehyde group (-CHO) and a carboxylic acid group (-COOH) attached to the thiophene ring, specifically at the 3 and 2 positions, respectively. The presence of these functional groups contributes to its reactivity and potential applications in organic synthesis and materials science. It is typically a solid at room temperature and may exhibit solubility in polar solvents due to the carboxylic acid group. The compound can participate in various chemical reactions, including condensation and esterification, making it useful in the synthesis of more complex molecules. Additionally, its unique structure allows for potential applications in the development of pharmaceuticals, agrochemicals, and as a building block in organic electronics. As with many thiophene derivatives, it may also exhibit interesting electronic properties, which can be exploited in various applications.

CAS 19991-68-5

3-formylthiophene-2-carboxylic acid

3-Formyl-2-thiophenecarboxylic acid

Ref: IN-DA002CFU

3-formylthiophene-2-carboxylic acid

Ref: 3D-UAA99168