CAS 101803-62-7

2,4,6-Tris(1-methylethyl)benzenesulfonyl fluoride

Description:

2,4,6-Tris(1-methylethyl)benzenesulfonyl fluoride, with the CAS number 101803-62-7, is a sulfonyl fluoride compound characterized by its unique structure, which includes a benzene ring substituted with three isopropyl groups and a sulfonyl fluoride functional group. This compound is typically a solid at room temperature and is known for its reactivity, particularly in nucleophilic substitution reactions due to the presence of the sulfonyl fluoride moiety. It is often utilized in organic synthesis and as a reagent in various chemical transformations, including the preparation of sulfonamides and other sulfonyl derivatives. The presence of the isopropyl groups contributes to its steric bulk, influencing its reactivity and solubility in organic solvents. Safety precautions are essential when handling this compound, as sulfonyl fluorides can be hazardous, potentially releasing toxic gases upon decomposition. Overall, 2,4,6-Tris(1-methylethyl)benzenesulfonyl fluoride is a valuable compound in synthetic organic chemistry, particularly in the development of pharmaceuticals and agrochemicals.

Formula: C₁₅H₂₃FO₂S

InChI: InChI=1S/C15H23FO2S/c1-9(2)12-7-13(10(3)4)15(19(16,17)18)14(8-12)11(5)6/h7-11H,1-6H3

InChI key: InChIKey=RTYWQCWRMCSZMD-UHFFFAOYSA-N

SMILES: S(F)(=O)(=O)C1=C(C(C)C)C=C(C(C)C)C=C1C(C)C

Synonyms:

• 2,4,6-Tris(1-methylethyl)benzenesulfonyl fluoride
• Benzenesulfonyl fluoride, 2,4,6-tris(1-methylethyl)-
• 2,4,6-Tris(propan-2-yl)benzene-1-sulfonyl fluoride
• 2,4,6-Triisopropylbenzenesulfonyl fluoride
• 2,4,6-Triisopropylbenzene-1-sulfonyl fluoride