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CAS 874219-31-5

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

Description:
[4-Fluoro-3-(pyrrolidine-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, making it valuable in various chemical reactions, particularly in Suzuki coupling reactions. The compound features a phenyl ring substituted with a fluorine atom and a pyrrolidine-1-carbonyl group, which contributes to its unique reactivity and potential biological activity. The boronic acid moiety enhances its solubility in polar solvents and allows for the formation of complexes with biomolecules, making it of interest in medicinal chemistry and drug development. Additionally, the presence of the pyrrolidine ring may impart specific conformational properties that can influence the compound's interaction with biological targets. Overall, this compound exemplifies the versatility of boronic acids in synthetic chemistry and their applications in pharmaceuticals and materials science.
Formula:C11H13BFNO3
InChI:InChI=1/C11H13BFNO3/c13-10-4-3-8(12(16)17)7-9(10)11(15)14-5-1-2-6-14/h3-4,7,16-17H,1-2,5-6H2
SMILES:C1CCN(C1)C(=O)c1cc(ccc1F)B(O)O
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