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CAS 352525-98-5

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6-Ethoxynaphthalen-2-yl boronic acid

Description:
6-Ethoxynaphthalen-2-yl boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a naphthalene derivative. This compound features an ethoxy group at the 6-position of the naphthalene ring, which contributes to its solubility and reactivity. Boronic acids are known for their ability to form reversible complexes with diols, making them valuable in various applications, including organic synthesis and medicinal chemistry. The presence of the boronic acid moiety allows for participation in Suzuki-Miyaura cross-coupling reactions, which are widely used for the formation of carbon-carbon bonds. Additionally, the ethoxy group can influence the electronic properties of the molecule, potentially enhancing its reactivity or selectivity in chemical reactions. Overall, 6-Ethoxynaphthalen-2-yl boronic acid is a versatile compound with applications in synthetic organic chemistry, particularly in the development of pharmaceuticals and advanced materials.
Formula:C12H13BO3
InChI:InChI=1S/C12H13BO3/c1-2-16-12-6-4-9-7-11(13(14)15)5-3-10(9)8-12/h3-8,14-15H,2H2,1H3
InChI key:InChIKey=INXXVGFSXYJGHI-UHFFFAOYSA-N
SMILES:O(CC)C1=CC2=C(C=C(B(O)O)C=C2)C=C1
Synonyms:
  • 6-Ethoxynaphthalen-2-yl boronic acid
  • B-(6-Ethoxy-2-naphthalenyl)boronic acid
  • Boronic Acid, B-(6-Ethoxy-2-Naphthalenyl)-
  • Boronic acid, (6-ethoxy-2-naphthalenyl)-
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