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CAS 874289-51-7

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[5-(tert-butylcarbamoyl)-2-fluoro-phenyl]boronic acid

Description:
[5-(tert-butylcarbamoyl)-2-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. The 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 affect its biological activity, while the fluorine atom can impart unique electronic properties. This compound is likely to exhibit moderate to high polarity due to the presence of the boronic acid and carbamoyl groups, making it soluble in polar solvents. Its boronic acid functionality allows it to participate in Suzuki-Miyaura cross-coupling reactions, making it valuable in the synthesis of complex organic molecules. Overall, this compound's unique structural features contribute to its potential applications in pharmaceuticals and materials science.
Formula:C11H15BFNO3
InChI:InChI=1/C11H15BFNO3/c1-11(2,3)14-10(15)7-4-5-9(13)8(6-7)12(16)17/h4-6,16-17H,1-3H3,(H,14,15)
SMILES:CC(C)(C)N=C(c1ccc(c(c1)B(O)O)F)O
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