2,3,5-Trifluorobenzenesulfonamide is an organic compound characterized by the presence of a sulfonamide functional group attached to a trifluorinated benzene ring. This compound features three fluorine atoms substituted at the 2, 3, and 5 positions of the benzene ring, which significantly influences its chemical properties, including increased electronegativity and potential reactivity. The sulfonamide group contributes to its solubility in polar solvents and can participate in hydrogen bonding, enhancing its biological activity. Typically, compounds like 2,3,5-trifluorobenzenesulfonamide are of interest in medicinal chemistry and materials science due to their unique electronic properties and potential applications in pharmaceuticals or agrochemicals. The presence of fluorine atoms often imparts desirable characteristics such as increased metabolic stability and lipophilicity. Safety data sheets should be consulted for handling and toxicity information, as fluorinated compounds can exhibit varying degrees of environmental persistence and biological effects. Overall, 2,3,5-trifluorobenzenesulfonamide represents a versatile compound with significant implications in various chemical research fields.

2,3,5-Trifluorobenzenesulfonamide

914637-01-7: Benzenesulfonamide, 2,3,5-trifluoro-, 2,3,5-Trifluorobenzenesulfonamide, 2,3,5-Trifluorobenzenesulphonamide, 2,3,5-Trifluorobenzene-1-sulfonamide

CAS 914637-01-7: 2,3,5-Trifluorobenzenesulfonamide

2,3,5-Trifluorobenzenesulphonamide

Ref: 10-F690519

2,3,5-Trifluorobenzenesulphonamide

Ref: 54-PC5068

2,3,5-TRIFLUOROBENZENESULPHONAMIDE

Ref: IN-DA01B31L