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CAS 1242339-88-3

:

3-(Chlorosulfonyl)-4-fluoro-5-methylbenzoic acid

Description:
3-(Chlorosulfonyl)-4-fluoro-5-methylbenzoic acid is an organic compound characterized by the presence of a benzoic acid structure with specific substituents that impart unique chemical properties. The compound features a chlorosulfonyl group, which enhances its reactivity, particularly in nucleophilic substitution reactions. The fluorine atom introduces electronegativity, influencing the compound's polarity and potential interactions with other molecules. The methyl group contributes to the hydrophobic character of the molecule, affecting its solubility in various solvents. This compound is likely to exhibit acidic behavior due to the carboxylic acid functional group, allowing it to participate in acid-base reactions. Its structural features suggest potential applications in pharmaceuticals or agrochemicals, where such functional groups can be pivotal for biological activity. Additionally, the presence of both electron-withdrawing and electron-donating groups can lead to interesting electronic properties, making it a candidate for further study in synthetic chemistry and material science. Safety and handling precautions should be observed due to the reactive nature of the chlorosulfonyl group.
Formula:C8H6ClFO4S
InChI:InChI=1S/C8H6ClFO4S/c1-4-2-5(8(11)12)3-6(7(4)10)15(9,13)14/h2-3H,1H3,(H,11,12)
InChI key:InChIKey=LJWWWHXBINZZCP-UHFFFAOYSA-N
SMILES:S(Cl)(=O)(=O)C1=CC(C(O)=O)=CC(C)=C1F
Synonyms:
  • 3-(Chlorosulfonyl)-4-fluoro-5-methylbenzoic acid
  • Benzoic acid, 3-(chlorosulfonyl)-4-fluoro-5-methyl-
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