4-Methoxy-2-(trifluoromethyl)benzenesulfonyl chloride, with the CAS number 775288-85-2, is an organic compound characterized by the presence of a sulfonyl chloride functional group attached to a benzene ring that is further substituted with a methoxy group and a trifluoromethyl group. 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 due to the sulfonyl chloride moiety, which can participate in nucleophilic substitution reactions. The trifluoromethyl group enhances the compound's electrophilicity and can influence its solubility and stability in various solvents. Additionally, the methoxy group can affect the electronic properties of the aromatic ring, making it more or less reactive towards electrophiles. This compound is often used in organic synthesis, particularly in the preparation of sulfonamides and other derivatives, and may also have applications in pharmaceuticals and agrochemicals. Proper handling and storage are essential due to its potential reactivity and toxicity.

Benzenesulfonyl chloride, 4-methoxy-2-(trifluoromethyl)-

775288-85-2: 4-Methoxy-2-(trifluoromethyl)benzenesulfonyl chloride, with the CAS number 775288-85-2, is an organic compound characterized by the presence of a sulfonyl chloride functional group attached to a benzene ring that is further substituted with a methoxy group and a trifluoromethyl group. 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 due to the sulfonyl chloride moiety, which can participate in nucleophilic substitution reactions. The trifluoromethyl group enhances the compound's electrophilicity and can influence its solubility and stability in various solvents. Additionally, the methoxy group can affect the electronic properties of the aromatic ring, making it more or less reactive towards electrophiles. This compound is often used in organic synthesis, particularly in the preparation of sulfonamides and other derivatives, and may also have applications in pharmaceuticals and agrochemicals. Proper handling and storage are essential due to its potential reactivity and toxicity.

4-Methoxy-2-(trifluoromethyl)benzenesulphonyl chloride

CAS 775288-85-2

Benzenesulfonyl chloride, 4-methoxy-2-(trifluoromethyl)-

4-Methoxy-2-(trifluoromethyl)benzenesulphonyl chloride

Ref: 54-PC302599