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CAS 192376-68-4

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3-Fluoro-4-propoxyphenylboronic acid

Description:
3-Fluoro-4-propoxyphenylboronic 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 fluorine atom and a propoxy group attached to a phenyl ring, which can influence its reactivity and solubility. The presence of the fluorine atom may enhance the compound's electronic properties, potentially affecting its interaction with biological targets. Boronic acids are often utilized in Suzuki coupling reactions, a key method for forming carbon-carbon bonds in organic synthesis. Additionally, the propoxy group can enhance the lipophilicity of the molecule, potentially improving its bioavailability in pharmaceutical applications. Overall, 3-Fluoro-4-propoxyphenylboronic acid is a versatile compound with significant implications in both synthetic and medicinal chemistry, particularly in the development of new therapeutic agents and materials.
Formula:C9H12BFO3
InChI:InChI=1/C9H12BFO3/c1-2-5-14-9-4-3-7(10(12)13)6-8(9)11/h3-4,6,12-13H,2,5H2,1H3
SMILES:CCCOc1ccc(cc1F)B(O)O
Synonyms:
  • 3-Fluor-4-Propoxyphenylboronic Acid
  • 3-Fluoro-4-propoxyphenylboroni
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