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CAS 854778-31-7

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4-Fluoro-3-methoxyphenylboronic acid

Description:
4-Fluoro-3-methoxyphenylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is substituted with both a fluorine atom and a methoxy group. This compound typically appears as a white to off-white solid and is soluble in polar organic solvents. The presence of the boronic acid group allows it to participate in various chemical reactions, particularly in Suzuki coupling reactions, which are essential in organic synthesis for forming carbon-carbon bonds. The fluorine atom can influence the electronic properties of the molecule, potentially enhancing its reactivity or selectivity in certain reactions. The methoxy group serves as an electron-donating substituent, which can stabilize the phenyl ring and affect the compound's overall reactivity. Additionally, this compound may exhibit interesting biological activities, making it a subject of interest in medicinal chemistry. Proper handling and storage are essential due to the potential reactivity of boronic acids with moisture and other nucleophiles.
Formula:C7H8BFO3
InChI:InChI=1S/C7H8BFO3/c1-12-7-4-5(8(10)11)2-3-6(7)9/h2-4,10-11H,1H3
InChI key:InChIKey=LUJMSRVFSBMEOY-UHFFFAOYSA-N
SMILES:O(C)C1=CC(B(O)O)=CC=C1F
Synonyms:
  • (4-Fluoro-3-methoxyphenyl)boronic acid
  • 3-Methoxy-4-fluorophenylboronic acid
  • 4-Fluoro-3-Methoxyphenylboronic
  • 4-Fluoro-3-methoxybenzeneboronic acid
  • 4-Fluoro-3-methoxyphenylboronic acid
  • 4-Fluoro-5-methoxyphenylboronic acid
  • B-(4-Fluoro-3-methoxyphenyl)boronic acid
  • Boronic acid, (4-fluoro-3-methoxyphenyl)-
  • boronic acid, B-(4-fluoro-3-methoxyphenyl)-
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