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CAS 139962-97-3

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(4-benzyloxy-2-formyl)phenyl boronic acid

Description:
(4-Benzyloxy-2-formyl)phenyl boronic acid is an organic compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The compound features a phenyl ring substituted with a benzyloxy group and an aldehyde group, contributing to its reactivity and potential for further functionalization. The boronic acid moiety enhances its utility in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is pivotal in the formation of carbon-carbon bonds. This compound may exhibit solubility in polar organic solvents, and its reactivity can be influenced by the presence of the electron-donating benzyloxy group. Additionally, the structural features suggest potential applications in the development of sensors or as intermediates in the synthesis of more complex organic molecules. Overall, (4-benzyloxy-2-formyl)phenyl boronic acid is a versatile compound with significant implications in synthetic organic chemistry.
Formula:C14H13BO4
InChI:InChI=1/C14H13BO4/c16-9-12-8-13(6-7-14(12)15(17)18)19-10-11-4-2-1-3-5-11/h1-9,17-18H,10H2
SMILES:c1ccc(cc1)COc1ccc(c(c1)C=O)B(O)O
Synonyms:
  • 264-717-2
  • Piperidine, 4,4'-(1,3-Propanediyl)Bis[1-Methyl-
  • 4,4'-Propane-1,3-Diylbis(1-Methylpiperidine)
  • [4-(Benzyloxy)-2-Formylphenyl]Boronic Acid
  • 4-Benzyloxy-2-formylphenylboronic acid
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