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CAS 499769-90-3

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B-2-Quinoxalinylboronic acid

Description:
B-2-Quinoxalinylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a quinoxaline moiety. This compound typically exhibits properties such as being a white to off-white solid, soluble in polar organic solvents, and possessing moderate stability under standard laboratory conditions. The boronic acid group allows for reversible covalent bonding with diols, making it useful in various applications, including medicinal chemistry and materials science. It can participate in Suzuki-Miyaura cross-coupling reactions, which are essential for synthesizing complex organic molecules. Additionally, the quinoxaline structure contributes to its potential biological activity, as quinoxalines are known for their diverse pharmacological properties. The compound's reactivity and functional versatility make it a valuable intermediate in organic synthesis and a candidate for further research in drug development and chemical biology. As with many boronic acids, care should be taken in handling due to potential reactivity with moisture and air.
Formula:C8H7BN2O2
InChI:InChI=1S/C8H7BN2O2/c12-9(13)8-5-10-6-3-1-2-4-7(6)11-8/h1-5,12-13H
InChI key:InChIKey=YZAMRPPXVOZTJJ-UHFFFAOYSA-N
SMILES:B(O)(O)C1=NC2=C(N=C1)C=CC=C2
Synonyms:
  • Boronic acid, 2-quinoxalinyl-
  • Boronic acid, B-2-quinoxalinyl-
  • (Quinoxalin-2-yl)boronic acid
  • B-2-Quinoxalinylboronic acid
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