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CAS 849833-86-9

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

Description:
[3-Fluoro-4-(methylcarbamoyl)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 methylcarbamoyl group, which contributes to its unique reactivity and potential biological activity. The fluorine atom can enhance the compound's lipophilicity and influence its interaction with biological targets. The methylcarbamoyl group may provide sites for hydrogen bonding, which can be crucial for binding interactions in biological systems. This compound is typically utilized in the development of pharmaceuticals, particularly in the synthesis of compounds that target specific enzymes or receptors. Its boronic acid moiety also makes it a valuable intermediate in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is essential for constructing complex organic molecules. Overall, [3-fluoro-4-(methylcarbamoyl)phenyl]boronic acid exhibits properties that make it significant in both synthetic and medicinal chemistry contexts.
Formula:C8H9BFNO3
InChI:InChI=1/C8H9BFNO3/c1-11-8(12)6-3-2-5(9(13)14)4-7(6)10/h2-4,13-14H,1H3,(H,11,12)
SMILES:CN=C(c1ccc(cc1F)B(O)O)O
Synonyms:
  • 3-Fluoro-4-methylcarbamoylphenylboronic acid
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