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CAS 279263-10-4

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(4-ethoxy-3-fluorophenyl)boronic acid

Description:
(4-Ethoxy-3-fluorophenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is further substituted with an ethoxy group and a fluorine atom. This compound typically exhibits a white to off-white solid appearance and is soluble in polar solvents such as water and alcohols, owing to the boronic acid moiety. The presence of the ethoxy group enhances its lipophilicity, while the fluorine atom can influence its electronic properties and reactivity. (4-Ethoxy-3-fluorophenyl)boronic acid is often utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, which are pivotal in the formation of carbon-carbon bonds. Its boronic acid functionality allows it to form reversible complexes with diols, making it useful in various applications, including drug development and materials science. Additionally, the compound's stability and reactivity can be influenced by environmental factors such as pH and temperature, which are important considerations in its handling and application.
Formula:C8H10BFO3
InChI:InChI=1/C8H10BFO3/c1-2-13-8-4-3-6(10)5-7(8)9(11)12/h3-5,11-12H,2H2,1H3
SMILES:CCOc1ccc(cc1B(O)O)F
Synonyms:
  • boronic acid, B-(4-ethoxy-3-fluorophenyl)-
  • (2-Ethoxy-5-Fluorophenyl)Boronic Acid
  • (4-Ethoxy-3-fluorophenyl)boronic acid
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