2-Chloro-5-(trifluoromethyl)benzenesulfonamide, with the CAS number 779-71-5, is an organic compound characterized by the presence of a sulfonamide functional group attached to a chlorinated aromatic ring. This compound features a chlorine atom at the 2-position and a trifluoromethyl group at the 5-position of the benzene ring, which significantly influences its chemical properties and reactivity. The trifluoromethyl group is known for imparting strong electron-withdrawing characteristics, enhancing the compound's acidity and potential reactivity in nucleophilic substitution reactions. The sulfonamide group contributes to its solubility in polar solvents and can also participate in hydrogen bonding. This compound is often utilized in pharmaceutical chemistry and agrochemical applications due to its biological activity and ability to act as a building block for more complex molecules. Safety data indicates that it should be handled with care, as it may pose health risks upon exposure. Overall, 2-chloro-5-(trifluoromethyl)benzenesulfonamide is a versatile compound with significant implications in various chemical research fields.

2-chloro-5-(trifluoromethyl)benzenesulfonamide

779-71-5: 2-Chloro-5-(trifluoromethyl)benzenesulfonamide, with the CAS number 779-71-5, is an organic compound characterized by the presence of a sulfonamide functional group attached to a chlorinated aromatic ring. This compound features a chlorine atom at the 2-position and a trifluoromethyl group at the 5-position of the benzene ring, which significantly influences its chemical properties and reactivity. The trifluoromethyl group is known for imparting strong electron-withdrawing characteristics, enhancing the compound's acidity and potential reactivity in nucleophilic substitution reactions. The sulfonamide group contributes to its solubility in polar solvents and can also participate in hydrogen bonding. This compound is often utilized in pharmaceutical chemistry and agrochemical applications due to its biological activity and ability to act as a building block for more complex molecules. Safety data indicates that it should be handled with care, as it may pose health risks upon exposure. Overall, 2-chloro-5-(trifluoromethyl)benzenesulfonamide is a versatile compound with significant implications in various chemical research fields.

CAS 779-71-5

2-chloro-5-(trifluoromethyl)benzenesulfonamide

2-Chloro-5-(trifluoromethyl)benzenesulfonamide

Ref: 54-PC1002619

2-Chloro-5-trifluoromethyl-benzenesulfonamide

Ref: 10-F033320