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CAS 874289-18-6

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[4-(tert-butylcarbamoyl)-3-fluoro-phenyl]boronic acid

Description:
[4-(tert-butylcarbamoyl)-3-fluoro-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. This compound features a phenyl ring substituted with a tert-butylcarbamoyl group and a fluorine atom, which can influence its reactivity and solubility. The tert-butylcarbamoyl moiety enhances the compound's stability and may improve its pharmacokinetic properties. The presence of the fluorine atom can also affect the electronic properties of the molecule, potentially enhancing its biological activity. As a boronic acid, it can participate in Suzuki coupling reactions, making it valuable in the synthesis of complex organic molecules. Additionally, the compound's solubility in various solvents and its ability to form complexes with biomolecules are important characteristics that can impact its application in drug development and materials science. Overall, this compound exemplifies the versatility of boronic acids in synthetic chemistry.
Formula:C11H15BFNO3
InChI:InChI=1/C11H15BFNO3/c1-11(2,3)14-10(15)8-5-4-7(12(16)17)6-9(8)13/h4-6,16-17H,1-3H3,(H,14,15)
SMILES:CC(C)(C)N=C(c1ccc(cc1F)B(O)O)O
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