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CAS 955369-43-4

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3-(2-hydroxypropan-2-yl)phenylboronic acid

Description:
3-(2-Hydroxypropan-2-yl)phenylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring, which is further substituted with a hydroxypropan-2-yl group. This compound typically exhibits properties such as solubility in polar solvents due to the hydroxyl group, and it can participate in various chemical reactions, including Suzuki coupling, which is significant in organic synthesis for forming carbon-carbon bonds. The boronic acid moiety allows for reversible interactions with diols, making it useful in biological applications, particularly in the development of sensors and drug delivery systems. Additionally, the compound may exhibit moderate acidity due to the boronic acid group, which can influence its reactivity and interactions in different environments. Its structural features contribute to its potential applications in medicinal chemistry and materials science, where it can serve as a building block for more complex molecules.
Formula:C9H13BO3
InChI:InChI=1S/C9H13BO3/c1-9(2,11)7-4-3-5-8(6-7)10(12)13/h3-6,11-13H,1-2H3
SMILES:CC(C)(c1cccc(c1)B(O)O)O
Synonyms:
  • [3-(2-Hydroxy-2-propanyl)phenyl]boronic acid
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