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CAS 871125-69-8

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B-(3-Ethoxy-2,4,6-trifluorophenyl)boronic acid

Description:
B-(3-Ethoxy-2,4,6-trifluorophenyl)boronic 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, particularly in organic synthesis and medicinal chemistry. The compound features a trifluorinated phenyl ring, which enhances its electronic properties and lipophilicity, potentially improving its reactivity and selectivity in chemical reactions. The ethoxy group contributes to the solubility and stability of the compound in organic solvents. This boronic acid derivative is often utilized in Suzuki-Miyaura cross-coupling reactions, facilitating the formation of carbon-carbon bonds, which is crucial in the synthesis of complex organic molecules. Additionally, the presence of fluorine atoms can influence the compound's biological activity and pharmacokinetics, making it of interest in drug discovery. Overall, B-(3-Ethoxy-2,4,6-trifluorophenyl)boronic acid exemplifies the versatility of boronic acids in synthetic chemistry and their potential applications in various fields.
Formula:C8H8BF3O3
InChI:InChI=1S/C8H8BF3O3/c1-2-15-8-5(11)3-4(10)6(7(8)12)9(13)14/h3,13-14H,2H2,1H3
InChI key:InChIKey=SGJHUHAGELVQDV-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(F)C(OCC)=C(F)C=C1F
Synonyms:
  • Boronic acid, B-(3-ethoxy-2,4,6-trifluorophenyl)-
  • Boronic acid, (3-ethoxy-2,4,6-trifluorophenyl)-
  • B-(3-Ethoxy-2,4,6-trifluorophenyl)boronic acid
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