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CAS 157033-24-4

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3,5-Difluorobenzeneacetyl chloride

Description:
3,5-Difluorobenzeneacetyl chloride is an organic compound characterized by the presence of both a benzene ring and an acetyl chloride functional group. The compound features two fluorine atoms positioned at the 3 and 5 positions of the benzene ring, which significantly influences its chemical reactivity and physical properties. As an acyl chloride, it is known for its high reactivity, particularly towards nucleophiles, making it useful in various synthetic applications, including the formation of amides and esters. The presence of fluorine atoms can enhance the compound's lipophilicity and alter its electronic properties, potentially affecting its behavior in chemical reactions. Typically, 3,5-difluorobenzeneacetyl chloride is a colorless to pale yellow liquid with a pungent odor, and it should be handled with care due to its corrosive nature and potential to release harmful gases upon reaction with water. Its applications may extend to pharmaceuticals, agrochemicals, and materials science, where it serves as an intermediate in the synthesis of more complex molecules.
Formula:C8H5ClF2O
InChI:InChI=1S/C8H5ClF2O/c9-8(12)3-5-1-6(10)4-7(11)2-5/h1-2,4H,3H2
InChI key:InChIKey=WMVPARKLYWQLNN-UHFFFAOYSA-N
SMILES:C(C(Cl)=O)C1=CC(F)=CC(F)=C1
Synonyms:
  • (3,5-Difluorophenyl)Acetyl Chloride
  • 2-(3,5-Difluorophenyl)acetyl chloride
  • 3,5-Difluorobenzeneacetyl chloride
  • Benzeneacetyl chloride, 3,5-difluoro-
  • 2-(3,5-Difluorophenyl)ethanoyl chloride
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