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CAS 1256345-79-5

:

B-(3-Hydroxy-5-methylphenyl)boronic acid

Description:
B-(3-Hydroxy-5-methylphenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenolic structure. This compound features a hydroxyl group and a methyl group on the aromatic ring, which contribute to its reactivity and solubility properties. Boronic acids are known for their ability to form reversible complexes with diols, making them valuable in various applications, including organic synthesis and medicinal chemistry. The presence of the hydroxyl group enhances its potential for hydrogen bonding, influencing its solubility in polar solvents. Additionally, the methyl group can affect the electronic properties of the aromatic ring, potentially influencing its reactivity in cross-coupling reactions, such as Suzuki-Miyaura coupling. This compound may also exhibit biological activity, making it of interest in pharmaceutical research. Overall, B-(3-Hydroxy-5-methylphenyl)boronic acid is a versatile compound with significant implications in both synthetic and medicinal chemistry.
Formula:C7H9BO3
InChI:InChI=1S/C7H9BO3/c1-5-2-6(8(10)11)4-7(9)3-5/h2-4,9-11H,1H3
InChI key:InChIKey=OYSWVVOTJWCGJA-UHFFFAOYSA-N
SMILES:B(O)(O)C1=CC(C)=CC(O)=C1
Synonyms:
  • 3-Hydroxy-5-methylphenylboronic acid
  • (3-Hydroxy-5-methylphenyl)boronic acid
  • Boronic acid, B-(3-hydroxy-5-methylphenyl)-
  • B-(3-Hydroxy-5-methylphenyl)boronic acid
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