2,6-Dimethylbenzenesulfonamide, with the CAS number 24010-56-8, is an organic compound that features a sulfonamide functional group attached to a dimethyl-substituted benzene ring. This compound is characterized by its aromatic structure, which contributes to its stability and reactivity. The presence of the sulfonamide group (-SO2NH2) imparts unique properties, including potential solubility in polar solvents and the ability to participate in various chemical reactions, such as nucleophilic substitutions. 2,6-Dimethylbenzenesulfonamide is typically a solid at room temperature and may exhibit moderate melting and boiling points due to its molecular interactions. It is often used in organic synthesis and may serve as an intermediate in the production of pharmaceuticals or agrochemicals. Additionally, the compound's structure allows for potential applications in medicinal chemistry, particularly in the development of sulfonamide-based drugs. Safety data should be consulted for handling and exposure guidelines, as with any chemical substance.

C8H11NO2S - InChI=1/C8H11NO2S/c1-6-4-3-5-7(2)8(6)12(9,10)11/h3-5H,1-2H3,(H2,9,10,11)

2,6-dimethylbenzenesulfonamide

24010-56-8: 2,6-Dimethylbenzenesulfonamide, with the CAS number 24010-56-8, is an organic compound that features a sulfonamide functional group attached to a dimethyl-substituted benzene ring. This compound is characterized by its aromatic structure, which contributes to its stability and reactivity. The presence of the sulfonamide group (-SO2NH2) imparts unique properties, including potential solubility in polar solvents and the ability to participate in various chemical reactions, such as nucleophilic substitutions. 2,6-Dimethylbenzenesulfonamide is typically a solid at room temperature and may exhibit moderate melting and boiling points due to its molecular interactions. It is often used in organic synthesis and may serve as an intermediate in the production of pharmaceuticals or agrochemicals. Additionally, the compound's structure allows for potential applications in medicinal chemistry, particularly in the development of sulfonamide-based drugs. Safety data should be consulted for handling and exposure guidelines, as with any chemical substance.

CAS 24010-56-8

2,6-dimethylbenzenesulfonamide

2,6-Dimethylbenzenesulfonamide

Ref: IN-DA00BLB7

2,6-Dimethylbenzene-1-sulfonamide

Ref: 3D-ZAA01056