
CAS 1092349-98-8
:2-Fluoro-3-methylbenzenesulfonylchloride
Description:
2-Fluoro-3-methylbenzenesulfonylchloride, with the CAS number 1092349-98-8, is an organosulfur compound characterized by the presence of a sulfonyl chloride functional group attached to a substituted aromatic ring. This compound features a fluorine atom and a methyl group positioned on the benzene ring, which influences its reactivity and physical properties. Typically, sulfonyl chlorides are known for their high reactivity, particularly in nucleophilic substitution reactions, making them valuable intermediates in organic synthesis. The presence of the fluorine atom can enhance the electrophilicity of the sulfonyl group, potentially increasing its reactivity towards nucleophiles. In terms of physical properties, compounds of this nature are often liquids or solids at room temperature, with varying solubility in organic solvents. Safety considerations are paramount, as sulfonyl chlorides can be corrosive and may release toxic gases upon reaction with water or amines. Overall, 2-Fluoro-3-methylbenzenesulfonylchloride serves as a useful reagent in the synthesis of pharmaceuticals and agrochemicals.
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Found 4 products.
2-FLUORO-3-METHYLBENZENESULFONYL CHLORIDE
CAS:Formula:C7H6ClFO2SPurity:98%Color and Shape:LiquidMolecular weight:208.63772-Fluoro-3-methylbenzenesulphonyl chloride
CAS:<p>2-Fluoro-3-methylbenzenesulphonyl chloride</p>Purity:≥95%Molecular weight:208.64g/mol2-Fluoro-3-methylbenzenesulfonyl chloride
CAS:Formula:C7H6ClFO2SPurity:99.0%Color and Shape:SolidMolecular weight:208.632-Fluoro-3-methylbenzenesulfonyl chloride
CAS:<p>Versatile small molecule scaffold</p>Formula:C7H6ClFO2SPurity:Min. 95%Molecular weight:208.63 g/mol



