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CAS 45713-46-0

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4-Methoxyphenylboronic acid

Description:
4-Methoxyphenylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a methoxy-substituted phenyl ring. Its molecular structure features a boron atom bonded to a hydroxyl group and a phenyl group that has a methoxy (-OCH₃) substituent in the para position. This compound is typically a white to off-white solid and is soluble in polar solvents such as water and alcohols, which enhances its utility in various chemical reactions. 4-Methoxyphenylboronic acid is known for its role in Suzuki-Miyaura cross-coupling reactions, making it valuable in organic synthesis, particularly in the formation of carbon-carbon bonds. Additionally, it can act as a ligand in coordination chemistry and has potential applications in medicinal chemistry due to its ability to interact with biological molecules. Its reactivity is influenced by the boronic acid group, which can form reversible complexes with diols, making it useful in sensor applications and drug delivery systems.
Formula:C7H9BO3
InChI:InChI=1/C7H9BO/c1-9-7-4-2-6(8)3-5-7/h2-5H,8H2,1H3
SMILES:COc1ccc(cc1)B
Synonyms:
  • (4-Methoxyphenyl)boronic acid
  • Boronic acid, B-(4-methoxyphenyl)-
  • 4-Methoxybenzeneboronic Acid
  • (4-Methoxyphenyl)Borane
  • Borane, (4-Methoxyphenyl)-
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