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CAS 355386-94-6

:

quinolin-5-yl-5-boronic acid

Description:
Quinolin-5-yl-5-boronic acid is an organic compound characterized by the presence of a quinoline moiety and a boronic acid functional group. The quinoline structure contributes to its aromatic properties, while the boronic acid group (-B(OH)2) is known for its ability to form reversible covalent bonds with diols, making it useful in various chemical reactions, particularly in Suzuki coupling reactions for the synthesis of biaryl compounds. This compound typically appears as a white to off-white solid and is soluble in polar solvents such as water and alcohols. Its boronic acid functionality allows it to participate in a range of chemical transformations, including cross-coupling reactions, which are valuable in medicinal chemistry and materials science. Additionally, quinolin-5-yl-5-boronic acid may exhibit biological activity, making it of interest in pharmaceutical research. Safety data should be consulted for handling and storage, as boronic acids can be sensitive to moisture and may require specific precautions.
Formula:C9H8BNO2
InChI:InChI=1/C9H8BNO2/c12-10(13)8-4-1-5-9-7(8)3-2-6-11-9/h1-6,12-13H
SMILES:c1cc(c2cccnc2c1)B(O)O
Synonyms:
  • Quinolin-5-Ylboronic Acid
  • Quinoline-5-Boronic Acid
  • 5-Quinolineboronic Acid
  • 5-Quinolinyl-Boronic Acid
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