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CAS 874219-43-9

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[3-fluoro-5-(piperidine-1-carbonyl)phenyl]boronic acid

Description:
[3-Fluoro-5-(piperidine-1-carbonyl)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 and is widely used in organic synthesis and medicinal chemistry. The compound features a phenyl ring substituted with a fluorine atom and a piperidine-derived carbonyl group, contributing to its unique chemical reactivity and potential biological activity. The presence of the piperidine moiety may enhance its solubility and interaction with biological targets. As a boronic acid, it can participate in Suzuki-Miyaura cross-coupling reactions, making it valuable in the synthesis of complex organic molecules. Additionally, the fluorine substitution can influence the electronic properties of the molecule, potentially affecting its pharmacokinetics and binding affinity in biological systems. Overall, this compound exemplifies the versatility of boronic acids in synthetic chemistry and their importance in drug development.
Formula:C12H15BFNO3
InChI:InChI=1/C12H15BFNO3/c14-11-7-9(6-10(8-11)13(17)18)12(16)15-4-2-1-3-5-15/h6-8,17-18H,1-5H2
SMILES:C1CCN(CC1)C(=O)c1cc(cc(c1)F)B(O)O
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