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CAS 1072951-45-1

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B-(5-Fluoro-8-quinolinyl)boronic acid

Description:
B-(5-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 5-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, the quinoline structure may impart biological activity, making this compound of interest in medicinal chemistry. Its boronic acid functionality allows for the formation of reversible covalent bonds with diols, which is significant in the development of sensors and drug delivery systems. Overall, B-(5-Fluoro-8-quinolinyl)boronic acid is a versatile compound with applications in both synthetic organic chemistry and pharmaceutical research.
Formula:C9H7BFNO2
InChI:InChI=1S/C9H7BFNO2/c11-8-4-3-7(10(13)14)9-6(8)2-1-5-12-9/h1-5,13-14H
InChI key:InChIKey=HWFXMAQYNZHRLY-UHFFFAOYSA-N
SMILES:B(O)(O)C=1C2=C(C(F)=CC1)C=CC=N2
Synonyms:
  • B-(5-Fluoro-8-quinolinyl)boronic acid
  • (5-Fluoroquinolin-8-yl)boronic acid
  • (5-Fluoroquinolin-8-yl)boronicacid
  • Boronic acid, B-(5-fluoro-8-quinolinyl)-
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