2-Cyclohexylethanesulfonamide, with the CAS number 4378-98-7, is an organic compound characterized by the presence of a sulfonamide functional group attached to a cyclohexyl ethyl chain. This compound typically exhibits properties associated with sulfonamides, such as being a solid at room temperature and possessing moderate solubility in polar solvents due to the sulfonamide group. The cyclohexyl moiety contributes to its hydrophobic characteristics, influencing its overall solubility and reactivity. 2-Cyclohexylethanesulfonamide may exhibit biological activity, as many sulfonamides are known for their antimicrobial properties, although specific biological data for this compound may vary. Its structure suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals. Additionally, the compound's stability and reactivity can be influenced by the presence of the sulfonamide group, which can participate in various chemical reactions, including nucleophilic substitutions. Overall, 2-cyclohexylethanesulfonamide represents a unique combination of structural features that may lend itself to diverse applications in chemical and pharmaceutical research.

2-cyclohexylethanesulfonamide

4378-98-7: 2-Cyclohexylethanesulfonamide, with the CAS number 4378-98-7, is an organic compound characterized by the presence of a sulfonamide functional group attached to a cyclohexyl ethyl chain. This compound typically exhibits properties associated with sulfonamides, such as being a solid at room temperature and possessing moderate solubility in polar solvents due to the sulfonamide group. The cyclohexyl moiety contributes to its hydrophobic characteristics, influencing its overall solubility and reactivity. 2-Cyclohexylethanesulfonamide may exhibit biological activity, as many sulfonamides are known for their antimicrobial properties, although specific biological data for this compound may vary. Its structure suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals. Additionally, the compound's stability and reactivity can be influenced by the presence of the sulfonamide group, which can participate in various chemical reactions, including nucleophilic substitutions. Overall, 2-cyclohexylethanesulfonamide represents a unique combination of structural features that may lend itself to diverse applications in chemical and pharmaceutical research.

CAS 4378-98-7

2-cyclohexylethanesulfonamide

2-Cyclohexylethane-1-sulfonamide

Ref: 3D-EAA37898