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CAS 1287753-39-2

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B-[4-(1-Ethoxyethyl)phenyl]boronic acid

Description:
B-[4-(1-Ethoxyethyl)phenyl]boronic acid is an organoboron 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 chemical applications, including organic synthesis and medicinal chemistry. The compound features a phenyl ring substituted with a 1-ethoxyethyl group, enhancing its solubility and reactivity. Boronic acids are typically polar, which contributes to their solubility in polar solvents, and they can participate in cross-coupling reactions, such as Suzuki-Miyaura coupling, facilitating the formation of carbon-carbon bonds. This specific boronic acid may also exhibit properties such as moderate acidity due to the boronic acid group, allowing it to act as a Lewis acid in certain reactions. Its unique structure and functional groups make it a valuable intermediate in the synthesis of pharmaceuticals and agrochemicals. As with many organoboron compounds, careful handling and storage are recommended due to potential reactivity and sensitivity to moisture.
Formula:C10H15BO3
InChI:InChI=1S/C10H15BO3/c1-3-14-8(2)9-4-6-10(7-5-9)11(12)13/h4-8,12-13H,3H2,1-2H3
InChI key:InChIKey=OUASAVPZGSGDFJ-UHFFFAOYSA-N
SMILES:C(OCC)(C)C1=CC=C(B(O)O)C=C1
Synonyms:
  • [4-(1-Ethoxyethyl)phenyl]boronic acid
  • Boronic acid, B-[4-(1-ethoxyethyl)phenyl]-
  • B-[4-(1-Ethoxyethyl)phenyl]boronic acid
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