3-Bromo-N-cyclohexyl-4-methylbenzenesulfonamide is a chemical compound characterized by its sulfonamide functional group, which is known for its antibacterial properties. The presence of the bromine atom at the 3-position of the aromatic ring contributes to its reactivity and potential applications in medicinal chemistry. The cyclohexyl group attached to the nitrogen atom enhances the lipophilicity of the molecule, potentially influencing its pharmacokinetic properties. The methyl group at the 4-position of the benzene ring can affect the compound's electronic properties and steric hindrance, which may play a role in its biological activity. This compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. Its structure suggests potential applications in drug development, particularly in the design of inhibitors targeting specific biological pathways. As with many sulfonamides, it may also exhibit a range of biological activities, making it of interest in pharmaceutical research. Safety and handling precautions should be observed due to the potential for toxicity associated with sulfonamide derivatives.

3-bromo-N-cyclohexyl-4-methylbenzenesulfonamide

850429-69-5: 3-Bromo-N-cyclohexyl-4-methylbenzenesulfonamide is a chemical compound characterized by its sulfonamide functional group, which is known for its antibacterial properties. The presence of the bromine atom at the 3-position of the aromatic ring contributes to its reactivity and potential applications in medicinal chemistry. The cyclohexyl group attached to the nitrogen atom enhances the lipophilicity of the molecule, potentially influencing its pharmacokinetic properties. The methyl group at the 4-position of the benzene ring can affect the compound's electronic properties and steric hindrance, which may play a role in its biological activity. This compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. Its structure suggests potential applications in drug development, particularly in the design of inhibitors targeting specific biological pathways. As with many sulfonamides, it may also exhibit a range of biological activities, making it of interest in pharmaceutical research. Safety and handling precautions should be observed due to the potential for toxicity associated with sulfonamide derivatives.

CAS 850429-69-5

3-bromo-N-cyclohexyl-4-methylbenzenesulfonamide

N-Cyclohexyl 3-bromo-4-methylbenzenesulfonamide

Ref: IN-DA003SWP