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CAS 874219-30-4

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[4-fluoro-3-(piperidine-1-carbonyl)phenyl]boronic acid

Description:
[4-Fluoro-3-(piperidine-1-carbonyl)phenyl]boronic acid is a boronic acid derivative characterized by the presence of a boron atom bonded to a phenyl ring that carries a fluorine substituent and a piperidine-1-carbonyl group. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The presence of the fluorine atom can enhance the compound's lipophilicity and influence its biological activity. Additionally, the piperidine moiety may contribute to the compound's pharmacological properties, potentially affecting its interaction with biological targets. As a boronic acid, it may also participate in Suzuki coupling reactions, a key method in the formation of carbon-carbon bonds in organic synthesis. Overall, this compound's unique structure and functional groups make it a valuable candidate for research in drug development and materials science.
Formula:C12H15BFNO3
InChI:InChI=1/C12H15BFNO3/c14-11-5-4-9(13(17)18)8-10(11)12(16)15-6-2-1-3-7-15/h4-5,8,17-18H,1-3,6-7H2
SMILES:C1CCN(CC1)C(=O)c1cc(ccc1F)B(O)O
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