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CAS 1706435-15-5

:

2-Fluoro-5-methoxy-3-(trifluoromethyl)benzenesulfonyl chloride

Description:
2-Fluoro-5-methoxy-3-(trifluoromethyl)benzenesulfonyl chloride is a specialized chemical compound characterized by its sulfonyl chloride functional group, which is known for its reactivity in various chemical reactions, particularly in the formation of sulfonamides and other derivatives. The presence of a trifluoromethyl group enhances its electrophilicity, making it a useful intermediate in organic synthesis. The fluorine substituents contribute to the compound's unique electronic properties, potentially affecting its solubility and reactivity. This compound is typically used in the synthesis of pharmaceuticals and agrochemicals, where precise modifications of aromatic systems are required. Additionally, the methoxy group can influence the compound's polarity and overall reactivity. As with many sulfonyl chlorides, it is important to handle this substance with care due to its potential to release hydrochloric acid upon reaction and its reactivity with water, which can lead to hydrolysis. Proper safety measures should be observed when working with this compound in a laboratory setting.
Formula:C8H5ClF4O3S
InChI:InChI=1S/C8H5ClF4O3S/c1-16-4-2-5(8(11,12)13)7(10)6(3-4)17(9,14)15/h2-3H,1H3
InChI key:InChIKey=OTELCLLTTDZQPW-UHFFFAOYSA-N
SMILES:C(F)(F)(F)C1=C(F)C(S(Cl)(=O)=O)=CC(OC)=C1
Synonyms:
  • 2-Fluoro-5-methoxy-3-(trifluoromethyl)benzenesulfonyl chloride
  • Benzenesulfonyl chloride, 2-fluoro-5-methoxy-3-(trifluoromethyl)-
  • 2-Fluoro-5-methoxy-3-(trifluoromethyl)benzenesulfonylchloride
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