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CAS 850589-53-6

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3-Ethoxy-5-fluorophenylboronic acid

Description:
3-Ethoxy-5-fluorophenylboronic 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 chemical reactions, particularly in Suzuki coupling reactions. This compound features a fluorine atom substituted on the phenyl ring, which can influence its electronic properties and reactivity. The ethoxy group enhances its solubility in organic solvents and may affect its steric and electronic characteristics. Typically, boronic acids like this one are utilized in organic synthesis, medicinal chemistry, and materials science due to their versatility in forming carbon-carbon bonds. The presence of the fluorine atom can also impart unique properties, such as increased lipophilicity or altered biological activity, making it of interest in pharmaceutical applications. Overall, 3-Ethoxy-5-fluorophenylboronic acid is a valuable compound in synthetic organic chemistry, with potential applications in drug development and materials science.
Formula:C8H10BFO3
InChI:InChI=1S/C8H10BFO3/c1-2-13-8-4-6(9(11)12)3-7(10)5-8/h3-5,11-12H,2H2,1H3
InChI key:InChIKey=OVVBLFYHZAMJIK-UHFFFAOYSA-N
SMILES:O(CC)C1=CC(B(O)O)=CC(F)=C1
Synonyms:
  • (3-Ethoxy-5-fluorophenyl)boronic acid
  • 3-Ethoxy-5-fluorophenylboronic acid
  • B-(3-Ethoxy-5-fluorophenyl)boronic acid
  • Boronic acid, (3-ethoxy-5-fluorophenyl)-
  • Boronic acid, B-(3-ethoxy-5-fluorophenyl)-
  • boronic acid, B-(3-ethoxy-5-fluorophenyl)-3-Ethoxy-5-Fluorophenylboronic Acid
  • 3-Fluoro-5-ethoxyphenylboronic acid
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