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CAS 874289-41-5

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[2-fluoro-5-(phenylcarbamoyl)phenyl]boronic acid

Description:
[2-Fluoro-5-(phenylcarbamoyl)phenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The compound features a fluorine atom and a phenylcarbamoyl group attached to a phenyl ring, contributing to its unique chemical reactivity and potential biological activity. Its structure allows for interactions with biological targets, which may be relevant in drug development. The boronic acid moiety can participate in Suzuki coupling reactions, facilitating the formation of carbon-carbon bonds, which is a valuable reaction in synthetic organic chemistry. Additionally, the presence of the fluorine atom may enhance the compound's lipophilicity and metabolic stability. Overall, [2-fluoro-5-(phenylcarbamoyl)phenyl]boronic acid is a versatile compound with applications in both synthetic methodologies and potential therapeutic contexts.
Formula:C13H11BFNO3
InChI:InChI=1/C13H11BFNO3/c15-12-7-6-9(8-11(12)14(18)19)13(17)16-10-4-2-1-3-5-10/h1-8,18-19H,(H,16,17)
SMILES:c1ccc(cc1)N=C(c1ccc(c(c1)B(O)O)F)O
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