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CAS 1218790-55-6

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B-[2-(Aminocarbonyl)-4-(trifluoromethyl)phenyl]boronic acid

Description:
B-[2-(Aminocarbonyl)-4-(trifluoromethyl)phenyl]boronic acid is a boronic acid derivative characterized by the presence of a boron atom bonded to a phenyl ring that features both an aminocarbonyl group and a trifluoromethyl substituent. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The aminocarbonyl group contributes to its potential as a building block in drug development, while the trifluoromethyl group enhances its lipophilicity and biological activity. The compound is likely to be a solid at room temperature and may exhibit moderate solubility in polar solvents. Its reactivity can be influenced by the presence of the boron atom, which can participate in cross-coupling reactions, making it valuable in the synthesis of complex organic molecules. Overall, this compound represents a versatile tool in both synthetic and medicinal chemistry contexts.
Formula:C8H7BF3NO3
InChI:InChI=1S/C8H7BF3NO3/c10-8(11,12)4-1-2-6(9(15)16)5(3-4)7(13)14/h1-3,15-16H,(H2,13,14)
InChI key:InChIKey=ZWBKNYWCDCOBOW-UHFFFAOYSA-N
SMILES:C(N)(=O)C1=C(B(O)O)C=CC(C(F)(F)F)=C1
Synonyms:
  • [2-Carbamoyl-4-(trifluoromethyl)phenyl]boronic acid
  • 2-Carbamoyl-4-(trifluoromethyl)phenylboronic acid
  • B-[2-(Aminocarbonyl)-4-(trifluoromethyl)phenyl]boronic acid
  • Boronic acid, B-[2-(aminocarbonyl)-4-(trifluoromethyl)phenyl]-
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