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CAS 156682-54-1

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3-Benzyloxyphenylboronic acid

Description:
3-Benzyloxyphenylboronic 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 benzyloxy group. This compound typically exhibits properties such as being a white to off-white solid at room temperature, with moderate solubility in polar organic solvents. The boronic acid moiety allows for reversible interactions with diols, making it useful in various applications, including organic synthesis and medicinal chemistry, particularly in the development of pharmaceuticals. Its structure enables it to participate in Suzuki-Miyaura cross-coupling reactions, which are pivotal in forming carbon-carbon bonds. Additionally, the presence of the benzyloxy group can enhance the compound's stability and solubility, facilitating its use in diverse chemical environments. As with many boronic acids, it may exhibit sensitivity to moisture and air, necessitating careful handling and storage conditions. Overall, 3-Benzyloxyphenylboronic acid serves as a valuable building block in synthetic organic chemistry.
Formula:C13H13BO3
InChI:InChI=1S/C13H13BO3/c15-14(16)12-7-4-8-13(9-12)17-10-11-5-2-1-3-6-11/h1-9,15-16H,10H2
InChI key:InChIKey=WIJNYNBSPQMJGO-UHFFFAOYSA-N
SMILES:O(CC1=CC=CC=C1)C2=CC(B(O)O)=CC=C2
Synonyms:
  • (3-Phenylmethoxyphenyl)boronic acid
  • 3-(Benzyloxy)-benzeneboronic acid
  • 3-Benzyloxyphenylboronic acid
  • B-[3-(Phenylmethoxy)phenyl]boronic acid
  • Boronic acid, B-[3-(phenylmethoxy)phenyl]-
  • Boronic acid, [3-(phenylmethoxy)phenyl]-
  • [3-[(Phenylmethyl)oxy]phenyl]boronic acid
  • 3-Benzyloxybenzeneboronic acid
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