4-Chloro-N-(2-hydroxyethyl)benzenesulfonamide, with the CAS number 6419-69-8, is a chemical compound characterized by its sulfonamide functional group, which is known for its antibacterial properties. This compound features a chloro substituent on the benzene ring, contributing to its reactivity and potential applications in medicinal chemistry. The presence of a hydroxyethyl group enhances its solubility in polar solvents and may influence its biological activity. Typically, sulfonamides exhibit a range of pharmacological effects, including antimicrobial activity, making them significant in the development of pharmaceuticals. The compound's structure suggests it may interact with biological systems through hydrogen bonding and other intermolecular forces, which can affect its efficacy and safety profile. Additionally, the chlorine atom may impart unique electronic properties, influencing the compound's reactivity and interactions with other molecules. Overall, 4-chloro-N-(2-hydroxyethyl)benzenesulfonamide is a compound of interest in both synthetic and medicinal chemistry, warranting further investigation into its potential applications.

4-chloro-N-(2-hydroxyethyl)benzenesulfonamide

6419-69-8: 4-Chloro-N-(2-hydroxyethyl)benzenesulfonamide, with the CAS number 6419-69-8, is a chemical compound characterized by its sulfonamide functional group, which is known for its antibacterial properties. This compound features a chloro substituent on the benzene ring, contributing to its reactivity and potential applications in medicinal chemistry. The presence of a hydroxyethyl group enhances its solubility in polar solvents and may influence its biological activity. Typically, sulfonamides exhibit a range of pharmacological effects, including antimicrobial activity, making them significant in the development of pharmaceuticals. The compound's structure suggests it may interact with biological systems through hydrogen bonding and other intermolecular forces, which can affect its efficacy and safety profile. Additionally, the chlorine atom may impart unique electronic properties, influencing the compound's reactivity and interactions with other molecules. Overall, 4-chloro-N-(2-hydroxyethyl)benzenesulfonamide is a compound of interest in both synthetic and medicinal chemistry, warranting further investigation into its potential applications.

CAS 6419-69-8

4-chloro-N-(2-hydroxyethyl)benzenesulfonamide

4-Chloro-N-(2-hydroxyethyl)benzenesulfonamide

Ref: IN-DA00ED86