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CAS 175276-61-6

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5-(4-Chlorophenyl)-2-(trifluoromethyl)furan-3-carbonyl chloride

Description:
5-(4-Chlorophenyl)-2-(trifluoromethyl)furan-3-carbonyl chloride is a chemical compound characterized by its unique structure, which includes a furan ring substituted with a chlorophenyl group and a trifluoromethyl group. This compound features a carbonyl chloride functional group, making it a reactive acyl chloride. The presence of the trifluoromethyl group enhances its lipophilicity and can influence its reactivity and biological activity. The chlorophenyl moiety contributes to the compound's potential applications in pharmaceuticals and agrochemicals, as it may exhibit specific interactions with biological targets. Additionally, the compound's reactivity as an acyl chloride allows it to participate in various chemical reactions, such as acylation and coupling reactions, making it valuable in synthetic organic chemistry. Its physical properties, such as melting point, boiling point, and solubility, would typically depend on the specific conditions and purity of the compound. Overall, this compound's unique structural features and functional groups suggest potential utility in various chemical applications.
Formula:C12H5Cl2F3O2
InChI:InChI=1S/C12H5Cl2F3O2/c13-7-3-1-6(2-4-7)9-5-8(11(14)18)10(19-9)12(15,16)17/h1-5H
InChI key:InChIKey=FOMUAOFXECJYNX-UHFFFAOYSA-N
SMILES:C(F)(F)(F)C1=C(C(Cl)=O)C=C(O1)C2=CC=C(Cl)C=C2
Synonyms:
  • 5-(4-Chlorophenyl)-2-(trifluoromethyl)-3-furancarbonyl chloride
  • 5-(4-Chlorophenyl)-2-trifluoromethylfuran-3-carbonyl chloride
  • 3-Furancarbonyl chloride, 5-(4-chlorophenyl)-2-(trifluoromethyl)-
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