4-Chloro-3-(1H-pyrrol-1-yl)benzoic acid is an organic compound characterized by its aromatic structure, which includes a benzoic acid moiety substituted with a chloro group and a pyrrole ring. The presence of the chloro substituent introduces a halogen, which can influence the compound's reactivity and solubility. The pyrrole ring contributes to the compound's potential biological activity, as pyrrole derivatives are often found in various natural products and pharmaceuticals. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar solvents due to the carboxylic acid functional group. Its chemical properties include the ability to participate in hydrogen bonding, which can affect its interactions in biological systems. Additionally, the compound may undergo various chemical reactions, such as electrophilic aromatic substitution or nucleophilic attacks, depending on the reaction conditions. Overall, 4-chloro-3-(1H-pyrrol-1-yl)benzoic acid is of interest in medicinal chemistry and material science due to its unique structural features and potential applications.

4-chloro-3-(1H-pyrrol-1-yl)benzoic acid

107946-72-5: 4-Chloro-3-(1H-pyrrol-1-yl)benzoic acid is an organic compound characterized by its aromatic structure, which includes a benzoic acid moiety substituted with a chloro group and a pyrrole ring. The presence of the chloro substituent introduces a halogen, which can influence the compound's reactivity and solubility. The pyrrole ring contributes to the compound's potential biological activity, as pyrrole derivatives are often found in various natural products and pharmaceuticals. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar solvents due to the carboxylic acid functional group. Its chemical properties include the ability to participate in hydrogen bonding, which can affect its interactions in biological systems. Additionally, the compound may undergo various chemical reactions, such as electrophilic aromatic substitution or nucleophilic attacks, depending on the reaction conditions. Overall, 4-chloro-3-(1H-pyrrol-1-yl)benzoic acid is of interest in medicinal chemistry and material science due to its unique structural features and potential applications.

CAS 107946-72-5

4-chloro-3-(1H-pyrrol-1-yl)benzoic acid

4-chloro-3-(1H-pyrrol-1-yl)benzoic acid

Ref: 10-F315011