5-Bromo-N-ethyl-2-methoxybenzenesulfonamide is a chemical compound characterized by its sulfonamide functional group, which is known for its antibacterial properties. The presence of a bromine atom at the 5-position of the benzene ring and an ethyl group attached to the nitrogen of the sulfonamide contributes to its unique reactivity and solubility profile. The methoxy group at the 2-position enhances the compound's lipophilicity, potentially influencing its biological activity and interaction with various targets. This compound may exhibit properties typical of sulfonamides, such as inhibition of bacterial folic acid synthesis, making it of interest in medicinal chemistry. Its molecular structure suggests potential applications in pharmaceuticals, particularly in the development of antimicrobial agents. Additionally, the presence of halogens and functional groups can affect its stability, solubility, and overall pharmacokinetic properties. As with many sulfonamides, careful consideration of its synthesis, handling, and biological effects is essential in research and application contexts.

5-bromo-N-ethyl-2-methoxybenzenesulfonamide

717892-29-0: 5-Bromo-N-ethyl-2-methoxybenzenesulfonamide is a chemical compound characterized by its sulfonamide functional group, which is known for its antibacterial properties. The presence of a bromine atom at the 5-position of the benzene ring and an ethyl group attached to the nitrogen of the sulfonamide contributes to its unique reactivity and solubility profile. The methoxy group at the 2-position enhances the compound's lipophilicity, potentially influencing its biological activity and interaction with various targets. This compound may exhibit properties typical of sulfonamides, such as inhibition of bacterial folic acid synthesis, making it of interest in medicinal chemistry. Its molecular structure suggests potential applications in pharmaceuticals, particularly in the development of antimicrobial agents. Additionally, the presence of halogens and functional groups can affect its stability, solubility, and overall pharmacokinetic properties. As with many sulfonamides, careful consideration of its synthesis, handling, and biological effects is essential in research and application contexts.

CAS 717892-29-0

5-bromo-N-ethyl-2-methoxybenzenesulfonamide

N-Ethyl 5-bromo-2-methoxybenzenesulfonamide

Ref: IN-DA005PTV

5-Bromo-N-ethyl-2-methoxybenzenesulphonamide

Ref: 54-OR9406