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CAS 313545-39-0

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4-Ethoxy-2-(trifluoromethyl)phenylboric acid

Description:
4-Ethoxy-2-(trifluoromethyl)phenylboric acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The compound features a trifluoromethyl group, which enhances its lipophilicity and can influence its biological activity. The ethoxy group contributes to the compound's solubility and reactivity. Typically, boronic acids like this one are utilized in Suzuki coupling reactions, a key method for forming carbon-carbon bonds in the synthesis of complex organic molecules. Additionally, the presence of fluorine atoms can impart unique electronic properties, potentially affecting the compound's reactivity and interaction with biological targets. Overall, 4-Ethoxy-2-(trifluoromethyl)phenylboric acid is a versatile compound with significant implications in both synthetic and medicinal chemistry.
Formula:C9H10BF3O3
InChI:InChI=1S/C9H10BF3O3/c1-2-16-6-3-4-8(10(14)15)7(5-6)9(11,12)13/h3-5,14-15H,2H2,1H3
InChI key:InChIKey=OGQUWAGSWMWDRG-UHFFFAOYSA-N
SMILES:C(F)(F)(F)C1=C(B(O)O)C=CC(OCC)=C1
Synonyms:
  • 4-Ethoxy-2-(trifluoromethyl)phenylboric acid
  • Boronic acid, [4-ethoxy-2-(trifluoromethyl)phenyl]-
  • [4-Ethoxy-2-trifluoromethylphenyl]boronic acid
  • boronic acid, B-[4-ethoxy-2-(trifluoromethyl)phenyl]-
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