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CAS 871125-78-9

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{4-[(naphthalen-1-yloxy)methyl]phenyl}boronic acid

Description:
{4-[(Naphthalen-1-yloxy)methyl]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 naphthalene moiety linked through an ether bond to a phenyl group, which is further substituted with a boronic acid group. This structure imparts unique properties, such as the potential for coordination with metal ions and participation in cross-coupling reactions, particularly in the formation of carbon-carbon bonds. The presence of the boronic acid group also allows for the formation of complexes with biomolecules, making it relevant in drug development and biochemical research. Additionally, the compound's solubility and stability can vary depending on the pH and the presence of other functional groups, influencing its reactivity and applications in various chemical processes. Overall, this compound exemplifies the versatility of boronic acids in synthetic and medicinal chemistry.
Formula:C17H15BO3
InChI:InChI=1/C17H15BO3/c19-18(20)15-10-8-13(9-11-15)12-21-17-7-3-5-14-4-1-2-6-16(14)17/h1-11,19-20H,12H2
SMILES:c1ccc2c(c1)cccc2OCc1ccc(cc1)B(O)O
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