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CAS 874289-16-4

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[3-fluoro-4-(isopropylcarbamoyl)phenyl]boronic acid

Description:
[3-fluoro-4-(isopropylcarbamoyl)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 an isopropylcarbamoyl group, which can influence its reactivity and solubility. The presence of the boronic acid moiety allows for participation in Suzuki-Miyaura cross-coupling reactions, making it valuable in the synthesis of complex organic molecules. Additionally, the fluorine atom can enhance the compound's biological activity and lipophilicity, potentially affecting its pharmacokinetic properties. The isopropylcarbamoyl group may contribute to the compound's stability and solubility in various solvents. Overall, this compound's unique structural features make it a significant candidate for research in drug development and materials science.
Formula:C10H13BFNO3
InChI:InChI=1/C10H13BFNO3/c1-6(2)13-10(14)8-4-3-7(11(15)16)5-9(8)12/h3-6,15-16H,1-2H3,(H,13,14)
SMILES:CC(C)N=C(c1ccc(cc1F)B(O)O)O
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