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CAS 190661-29-1

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(2-Benzyloxyphenyl)boronic acid

Description:
(2-Benzyloxyphenyl)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 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 like methanol and ethanol, while being less soluble in non-polar solvents. 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, particularly in the development of pharmaceuticals. Additionally, it can participate in Suzuki-Miyaura cross-coupling reactions, which are vital for constructing complex organic molecules. The presence of the benzyloxy group can enhance the compound's stability and influence its reactivity. Overall, (2-Benzyloxyphenyl)boronic acid serves as a valuable building block in synthetic organic chemistry due to its unique reactivity and functional versatility.
Formula:C13H13BO3
InChI:InChI=1/C13H13BO3/c15-14(16)12-8-4-5-9-13(12)17-10-11-6-2-1-3-7-11/h1-9,15-16H,10H2
SMILES:c1ccc(cc1)COc1ccccc1B(O)O
Synonyms:
  • 2-Benzyloxyphenylboronic acid
  • 2-Benzyloxybenzeneboronic acid
  • 2-Phenylmethoxy Phenylboronic Acid
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