3-(2-Iodobenzamido)thiophene-2-carboxylic acid is an organic compound characterized by its unique structure, which includes a thiophene ring, an amide functional group, and a carboxylic acid group. The presence of the iodine atom in the 2-position of the benzamide moiety enhances its reactivity and potential for various chemical transformations. This compound is likely to exhibit properties typical of thiophene derivatives, such as good solubility in organic solvents and potential for π-π stacking interactions due to its aromatic nature. The carboxylic acid group contributes to its acidity and can participate in hydrogen bonding, influencing its solubility and reactivity in biological systems. Additionally, the compound may exhibit interesting biological activities, making it a candidate for pharmaceutical applications. Its specific characteristics, such as melting point, boiling point, and spectral data, would require empirical measurement or literature reference for precise values. Overall, 3-(2-iodobenzamido)thiophene-2-carboxylic acid represents a versatile scaffold in organic synthesis and medicinal chemistry.

3-(2-iodobenzamido)thiophene-2-carboxylic acid

926186-87-0: 3-(2-Iodobenzamido)thiophene-2-carboxylic acid is an organic compound characterized by its unique structure, which includes a thiophene ring, an amide functional group, and a carboxylic acid group. The presence of the iodine atom in the 2-position of the benzamide moiety enhances its reactivity and potential for various chemical transformations. This compound is likely to exhibit properties typical of thiophene derivatives, such as good solubility in organic solvents and potential for π-π stacking interactions due to its aromatic nature. The carboxylic acid group contributes to its acidity and can participate in hydrogen bonding, influencing its solubility and reactivity in biological systems. Additionally, the compound may exhibit interesting biological activities, making it a candidate for pharmaceutical applications. Its specific characteristics, such as melting point, boiling point, and spectral data, would require empirical measurement or literature reference for precise values. Overall, 3-(2-iodobenzamido)thiophene-2-carboxylic acid represents a versatile scaffold in organic synthesis and medicinal chemistry.

3-(2-Iodobenzamido)thiophene-2-carboxylic acid is a research tool that is used in the study of protein interactions. The chemical structure of 3-(2-Iodobenzamido)thiophene-2-carboxylic acid includes a thiophene ring and two amide groups, which can be used to inhibit ion channels and ligand binding. The CAS number for 3-(2-Iodobenzamido)thiophene-2-carboxylic acid is 926186-87-0. This compound has been shown to activate proteins by binding to them. 3-(2-Iodobenzamido)thiophene-2-carboxylic acid has also been shown to inhibit the activity of an antibody.

CAS 926186-87-0

3-(2-iodobenzamido)thiophene-2-carboxylic acid

3-(2-Iodobenzamido)thiophene-2-carboxylic acid

Ref: 3D-BMB18687