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CAS 874289-13-1

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

Description:
[4-(Dimethylcarbamoyl)-3-fluoro-phenyl]boronic acid is an organic 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 dimethylcarbamoyl group and a fluorine atom, which can influence its reactivity and biological activity. The dimethylcarbamoyl moiety may enhance solubility and stability, while the fluorine atom can affect the electronic properties of the molecule, potentially increasing its lipophilicity. This compound may be utilized in various applications, including drug development and as a building block in the synthesis of more complex molecules. Its boronic acid functionality allows for participation in Suzuki coupling reactions, making it valuable in the formation of carbon-carbon bonds. Overall, the unique combination of functional groups in [4-(dimethylcarbamoyl)-3-fluoro-phenyl]boronic acid contributes to its versatility in chemical synthesis and potential therapeutic applications.
Formula:C9H11BFNO3
InChI:InChI=1/C9H11BFNO3/c1-12(2)9(13)7-4-3-6(10(14)15)5-8(7)11/h3-5,14-15H,1-2H3
SMILES:CN(C)C(=O)c1ccc(cc1F)B(O)O
Synonyms:
  • [4-(Dimethylcarbamoyl)-3-Fluorophenyl]Boronic Acid
  • 4-(Dimethylcarbamoyl)-3-Fluorobenzeneboronic Acid
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