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CAS 1698028-43-1

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B-(3-Hydroxy-1-naphthalenyl)boronic acid

Description:
B-(3-Hydroxy-1-naphthalenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a naphthalene derivative. This compound typically exhibits properties such as solubility in polar organic solvents and moderate stability under ambient conditions. The hydroxyl group on the naphthalene ring enhances its reactivity, making it useful in various chemical reactions, particularly in Suzuki-Miyaura cross-coupling reactions, which are pivotal in organic synthesis for forming carbon-carbon bonds. Additionally, the boronic acid moiety allows for the formation of reversible complexes with diols, which can be exploited in sensor applications and drug delivery systems. The compound may also exhibit fluorescence properties, making it valuable in materials science and biological imaging. Its structural features contribute to its potential applications in medicinal chemistry, particularly in the development of pharmaceuticals targeting specific biological pathways. Overall, B-(3-Hydroxy-1-naphthalenyl)boronic acid is a versatile compound with significant implications in both synthetic and applied chemistry.
Formula:C10H9BO3
InChI:InChI=1S/C10H9BO3/c12-8-5-7-3-1-2-4-9(7)10(6-8)11(13)14/h1-6,12-14H
InChI key:InChIKey=OJCMZQBOMVSRMS-UHFFFAOYSA-N
SMILES:B(O)(O)C=1C2=C(C=C(O)C1)C=CC=C2
Synonyms:
  • Boronic acid, B-(3-hydroxy-1-naphthalenyl)-
  • B-(3-Hydroxy-1-naphthalenyl)boronic acid
  • (3-Hydroxynaphthalen-1-yl)boronic acid
  • 3-Hydroxynaphthalene-1-boronic Acid
  • 3-hydroxynaphthalen-1-yl-1-boronic acid
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