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CAS 1437769-83-9

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3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-2-naphthalenol

Description:
3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-2-naphthalenol is a chemical compound characterized by its unique structure, which includes a naphthol moiety and a boron-containing dioxaborolane group. This compound typically exhibits properties associated with both aromatic compounds and boron derivatives, such as potential fluorescence and reactivity in various chemical transformations. The presence of the dioxaborolane group suggests that it may participate in reactions typical of boron compounds, including cross-coupling reactions, making it valuable in organic synthesis and materials science. Additionally, the hydroxyl group in the naphthalene structure can engage in hydrogen bonding, influencing its solubility and interaction with other molecules. The compound's stability and reactivity can be affected by the steric hindrance introduced by the tetramethyl groups, which may also impact its physical properties, such as melting point and solubility in different solvents. Overall, this compound is of interest in fields such as medicinal chemistry and organic synthesis due to its functional groups and potential applications.
Formula:C16H19BO3
InChI:InChI=1S/C16H19BO3/c1-15(2)16(3,4)20-17(19-15)13-9-11-7-5-6-8-12(11)10-14(13)18/h5-10,18H,1-4H3
InChI key:InChIKey=ABMLEYBIIGSGCL-UHFFFAOYSA-N
SMILES:OC=1C(=CC2=C(C1)C=CC=C2)B3OC(C)(C)C(C)(C)O3
Synonyms:
  • 3-Hydroxynaphthalene-2-boronic acid pinacol ester
  • 2-Naphthalenol, 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
  • 3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-2-naphthalenol
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