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CAS 874288-06-9

:

B-[4-[[(2-Fluorophenyl)amino]carbonyl]phenyl]boronic acid

Description:
B-[4-[[(2-Fluorophenyl)amino]carbonyl]phenyl]boronic acid, identified by its CAS number 874288-06-9, is a boronic acid derivative characterized by the presence of a boron atom bonded to a phenyl group and an amino acid moiety. This compound features a fluorinated phenyl ring, which enhances its electronic properties and potential reactivity. The boronic acid functional group is known for its ability to form reversible covalent bonds with diols, making it valuable in various applications, including organic synthesis and medicinal chemistry. The presence of the amino and carbonyl groups contributes to its potential as a building block in drug development, particularly in the design of protease inhibitors or other therapeutic agents. Additionally, the compound's solubility and stability in various solvents can be influenced by the substituents on the aromatic rings. Overall, this compound exemplifies the versatility of boronic acids in chemical synthesis and their role in biological systems.
Formula:C13H11BFNO3
InChI:InChI=1S/C13H11BFNO3/c15-11-3-1-2-4-12(11)16-13(17)9-5-7-10(8-6-9)14(18)19/h1-8,18-19H,(H,16,17)
InChI key:InChIKey=IMEVTROIYKNWMT-UHFFFAOYSA-N
SMILES:C(NC1=C(F)C=CC=C1)(=O)C2=CC=C(B(O)O)C=C2
Synonyms:
  • Boronic acid, B-[4-[[(2-fluorophenyl)amino]carbonyl]phenyl]-
  • B-[4-[[(2-Fluorophenyl)amino]carbonyl]phenyl]boronic acid
  • Boronic acid, [4-[[(2-fluorophenyl)amino]carbonyl]phenyl]-
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