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CAS 184000-11-1

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(4-Benzyloxycarbonylphenyl)boronic acid

Description:
(4-Benzyloxycarbonylphenyl)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 benzyloxycarbonyl group. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible complexes with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The presence of the benzyloxycarbonyl group enhances its stability and solubility in organic solvents. Additionally, this compound may participate in Suzuki-Miyaura cross-coupling reactions, which are valuable for constructing carbon-carbon bonds in the synthesis of complex organic molecules. Its structure allows for potential applications in drug development and materials science, particularly in the design of sensors or catalysts. As with many boronic acids, it is important to handle this compound with care, as it may be sensitive to moisture and air, which can affect its reactivity and stability.
Formula:C14H13BO4
InChI:InChI=1/C14H13BO4/c16-14(19-10-11-4-2-1-3-5-11)12-6-8-13(9-7-12)15(17)18/h1-9,17-18H,10H2
SMILES:c1ccc(cc1)COC(=O)c1ccc(cc1)B(O)O
Synonyms:
  • Benzyl 4-boronobenzoat
  • {4-[(Benzyloxy)Carbonyl]Phenyl}Boronic Acid
  • 4-Benzyloxycarbonylphenyl boronic acid
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