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CAS 874219-33-7

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[4-fluoro-3-(phenylcarbamoyl)phenyl]boronic acid

Description:
[4-Fluoro-3-(phenylcarbamoyl)phenyl]boronic acid is a boronic acid derivative characterized by the presence of a boron atom bonded to a phenyl group and a carboxylic acid functional group. This compound features a fluorine atom at the para position relative to the boronic acid group, which can influence its reactivity and solubility. The phenylcarbamoyl moiety contributes to its potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, as it may interact with biological targets through hydrogen bonding and π-π stacking interactions. Boronic acids are known for their ability to form reversible covalent bonds with diols, making them useful in various applications, including drug delivery and sensor technology. The compound's solubility, stability, and reactivity can be influenced by the presence of the fluorine atom and the overall molecular structure. As with many boronic acids, it may also exhibit unique properties in catalytic reactions, particularly in cross-coupling reactions in organic synthesis.
Formula:C13H11BFNO3
InChI:InChI=1/C13H11BFNO3/c15-12-7-6-9(14(18)19)8-11(12)13(17)16-10-4-2-1-3-5-10/h1-8,18-19H,(H,16,17)
SMILES:c1ccc(cc1)N=C(c1cc(ccc1F)B(O)O)O
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