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CAS 871332-66-0

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B-[3-(Aminocarbonyl)-5-fluorophenyl]boronic acid

Description:
B-[3-(Aminocarbonyl)-5-fluorophenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is substituted with both an aminocarbonyl and a fluorine atom. This compound typically exhibits properties such as being a white to off-white solid, with solubility in polar solvents like water and alcohols due to the boronic acid moiety. The aminocarbonyl group contributes to its potential as a building block in medicinal chemistry, particularly in the development of pharmaceuticals, as it can participate in various chemical reactions, including Suzuki coupling. The fluorine atom enhances the compound's lipophilicity and may influence its biological activity. Additionally, boronic acids are known for their ability to form reversible complexes with diols, which can be exploited in drug delivery systems and sensor applications. Overall, B-[3-(Aminocarbonyl)-5-fluorophenyl]boronic acid is a versatile compound with significant implications in organic synthesis and medicinal chemistry.
Formula:C7H7BFNO3
InChI:InChI=1S/C7H7BFNO3/c9-6-2-4(7(10)11)1-5(3-6)8(12)13/h1-3,12-13H,(H2,10,11)
InChI key:InChIKey=FTMWTTRIUYYHDE-UHFFFAOYSA-N
SMILES:B(O)(O)C1=CC(C(N)=O)=CC(F)=C1
Synonyms:
  • B-[3-(Aminocarbonyl)-5-fluorophenyl]boronic acid
  • Boronic acid, [3-(aminocarbonyl)-5-fluorophenyl]-
  • 3-Carbamoyl-5-fluorophenylboronic acid
  • Boronic acid, B-[3-(aminocarbonyl)-5-fluorophenyl]-
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