4-Fluoro-2,6-dimethylbenzenesulfonyl chloride, with the CAS number 88972-03-6, is an aromatic sulfonyl chloride characterized by the presence of a sulfonyl group (-SO2Cl) attached to a benzene ring that is further substituted with a fluorine atom and two methyl groups. This compound typically appears as a colorless to pale yellow liquid or solid, depending on its purity and temperature. It is known for its reactivity, particularly in nucleophilic substitution reactions, where the sulfonyl chloride group can act as a leaving group. The presence of the fluorine atom can influence the electronic properties of the molecule, enhancing its electrophilicity. As a sulfonyl chloride, it is also sensitive to moisture and can hydrolyze to form the corresponding sulfonic acid. This compound is utilized in organic synthesis, particularly in the preparation of various pharmaceuticals and agrochemicals, due to its ability to introduce sulfonyl groups into other organic molecules. Proper handling and storage are essential, as it can be corrosive and may pose health hazards.

Benzenesulfonyl chloride, 4-fluoro-2,6-dimethyl-

88972-03-6: 4-Fluoro-2,6-dimethylbenzenesulfonyl chloride, with the CAS number 88972-03-6, is an aromatic sulfonyl chloride characterized by the presence of a sulfonyl group (-SO2Cl) attached to a benzene ring that is further substituted with a fluorine atom and two methyl groups. This compound typically appears as a colorless to pale yellow liquid or solid, depending on its purity and temperature. It is known for its reactivity, particularly in nucleophilic substitution reactions, where the sulfonyl chloride group can act as a leaving group. The presence of the fluorine atom can influence the electronic properties of the molecule, enhancing its electrophilicity. As a sulfonyl chloride, it is also sensitive to moisture and can hydrolyze to form the corresponding sulfonic acid. This compound is utilized in organic synthesis, particularly in the preparation of various pharmaceuticals and agrochemicals, due to its ability to introduce sulfonyl groups into other organic molecules. Proper handling and storage are essential, as it can be corrosive and may pose health hazards.

4-Fluoro-2,6-dimethylbenzene-1-sulfonyl chloride

CAS 88972-03-6

Benzenesulfonyl chloride, 4-fluoro-2,6-dimethyl-

Benzenesulfonyl chloride, 4-fluoro-2,6-dimethyl-

Ref: IN-DA0046V8

4-Fluoro-2,6-dimethylbenzene-1-sulfonyl chloride

Ref: 54-PC1007501