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CAS 850568-48-8

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B-[4-(3-Hydroxypropyl)phenyl]boronic acid

Description:
B-[4-(3-Hydroxypropyl)phenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is further substituted with a hydroxypropyl group. This compound typically exhibits properties such as solubility in polar solvents due to the hydroxyl group, which can engage in hydrogen bonding. The boronic acid moiety allows for the formation of reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. It can participate in Suzuki-Miyaura cross-coupling reactions, which are vital for constructing complex organic molecules. Additionally, the presence of the hydroxypropyl group may enhance its biological activity and solubility profile. The compound's structure suggests potential applications in drug development, particularly in targeting specific biological pathways or as a building block in the synthesis of more complex molecules. As with many boronic acids, it may also exhibit pH-dependent behavior, influencing its reactivity and stability in different environments.
Formula:C9H13BO3
InChI:InChI=1S/C9H13BO3/c11-7-1-2-8-3-5-9(6-4-8)10(12)13/h3-6,11-13H,1-2,7H2
InChI key:InChIKey=KCRVWMBFIDPDIF-UHFFFAOYSA-N
SMILES:B(O)(O)C1=CC=C(CCCO)C=C1
Synonyms:
  • B-[4-(3-Hydroxypropyl)phenyl]boronic acid
  • Boronic acid, [4-(3-hydroxypropyl)phenyl]-
  • boronic acid, B-[4-(3-hydroxypropyl)phenyl]-
  • [4-(3-Hydroxypropyl)phenyl]boronic acid
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