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CAS 1072951-44-0

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B-(6-Fluoro-8-quinolinyl)boronic acid

Description:
B-(6-Fluoro-8-quinolinyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a quinoline derivative. This compound typically exhibits properties such as moderate solubility in polar organic solvents and potential reactivity with various electrophiles due to the boronic acid moiety. The fluorine atom in the 6-position of the quinoline ring can influence the electronic properties and reactivity of the molecule, potentially enhancing its ability to participate in Suzuki coupling reactions, which are widely used in organic synthesis for forming carbon-carbon bonds. Additionally, boronic acids are known for their ability to form reversible complexes with diols, making them useful in various applications, including drug development and materials science. The specific structural features of B-(6-Fluoro-8-quinolinyl)boronic acid may also contribute to its biological activity, making it a subject of interest in medicinal chemistry. Overall, this compound exemplifies the versatility of boronic acids in synthetic and medicinal chemistry.
Formula:C9H7BFNO2
InChI:InChI=1S/C9H7BFNO2/c11-7-4-6-2-1-3-12-9(6)8(5-7)10(13)14/h1-5,13-14H
InChI key:InChIKey=LZPMJHIHYGRDJX-UHFFFAOYSA-N
SMILES:B(O)(O)C=1C2=C(C=C(F)C1)C=CC=N2
Synonyms:
  • (6-Fluoroquinolin-8-yl)boronic acid
  • B-(6-Fluoro-8-quinolinyl)boronic acid
  • Boronic acid, B-(6-fluoro-8-quinolinyl)-
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