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CAS 259209-25-1

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B-(2-Hydroxy-4-methylphenyl)boronic acid

Description:
B-(2-Hydroxy-4-methylphenyl)boronic acid, with the CAS number 259209-25-1, is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenolic structure. This compound typically exhibits a white to off-white crystalline appearance and is soluble in polar solvents such as water and alcohols, owing to the hydroxyl group. The boronic acid moiety allows for the formation of reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and as a reagent in Suzuki coupling reactions. Additionally, the presence of the methyl and hydroxyl substituents on the aromatic ring can influence its reactivity and solubility, enhancing its utility in medicinal chemistry and materials science. B-(2-Hydroxy-4-methylphenyl)boronic acid is also of interest in the development of sensors and drug delivery systems due to its ability to interact with biological molecules. Overall, its unique structural features contribute to its versatility in chemical research and applications.
Formula:C7H9BO3
InChI:InChI=1S/C7H9BO3/c1-5-2-3-6(8(10)11)7(9)4-5/h2-4,9-11H,1H3
InChI key:InChIKey=JHCQENHEMNQVSO-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(O)C=C(C)C=C1
Synonyms:
  • Boronic acid, B-(2-hydroxy-4-methylphenyl)-
  • Boronic acid, (2-hydroxy-4-methylphenyl)-
  • B-(2-Hydroxy-4-methylphenyl)boronic acid
  • (2-Hydroxy-4-methylphenyl)boronic acid
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