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CAS 874288-39-8

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B-[4-(Aminocarbonyl)-3-fluorophenyl]boronic acid

Description:
B-[4-(Aminocarbonyl)-3-fluorophenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that features both an amino and a fluorine substituent. This compound typically exhibits properties such as being a white to off-white solid, soluble in polar solvents like water and methanol, and possessing moderate stability under standard conditions. The boronic acid moiety allows for participation in various chemical reactions, particularly in Suzuki coupling reactions, making it valuable in organic synthesis and medicinal chemistry. The amino group can engage in hydrogen bonding and may enhance the compound's biological activity, while the fluorine atom can influence the electronic properties and lipophilicity of the molecule. Overall, this compound is of interest in the development of pharmaceuticals and agrochemicals due to its potential reactivity and biological interactions.
Formula:C7H7BFNO3
InChI:InChI=1S/C7H7BFNO3/c9-6-3-4(8(12)13)1-2-5(6)7(10)11/h1-3,12-13H,(H2,10,11)
InChI key:InChIKey=LKXXEWDYAWOZRW-UHFFFAOYSA-N
SMILES:B(O)(O)C1=CC(F)=C(C(N)=O)C=C1
Synonyms:
  • 4-Carbamoyl-3-fluorobenzeneboronic acid
  • B-[4-(Aminocarbonyl)-3-fluorophenyl]boronic acid
  • Boronic acid, B-[4-(aminocarbonyl)-3-fluorophenyl]-
  • Boronic acid, [4-(aminocarbonyl)-3-fluorophenyl]-
  • [4-(Aminocarbonyl)-3-fluorophenyl]boronic acid
  • 4-Carbamoyl-3-fluorophenylboronic acid
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