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CAS 886853-93-6

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(2-methoxyquinolin-3-yl)boronic acid

Description:
(2-Methoxyquinolin-3-yl)boronic acid is an organic compound characterized by the presence of a boronic acid functional group attached to a quinoline ring system. This compound features a methoxy group at the 2-position of the quinoline, which contributes to its solubility and reactivity. Boronic acids are known for their ability to form reversible covalent bonds with diols, making them valuable in various applications, including organic synthesis and medicinal chemistry. The presence of the quinoline moiety suggests potential biological activity, as quinolines are often found in pharmaceuticals and exhibit diverse pharmacological properties. Additionally, (2-methoxyquinolin-3-yl)boronic acid may serve as a useful intermediate in the synthesis of more complex molecules or as a ligand in coordination chemistry. Its properties, such as solubility, stability, and reactivity, can be influenced by the specific substituents on the quinoline ring and the boronic acid group, making it a compound of interest in both research and industrial applications.
Formula:C10H10BNO3
InChI:InChI=1/C10H10BNO3/c1-15-10-8(11(13)14)6-7-4-2-3-5-9(7)12-10/h2-6,13-14H,1H3
SMILES:COc1c(cc2ccccc2n1)B(O)O
Synonyms:
  • Boronic acid, B-(2-methoxy-3-quinolinyl)-
  • (2-Methoxyquinolin-3-yl)boronic acid
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