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CAS 874288-35-4

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[3-[(2-fluorophenyl)carbamoyl]phenyl]boronic acid

Description:
[3-[(2-fluorophenyl)carbamoyl]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. This compound features a phenyl ring substituted with a carbamoyl group and a fluorophenyl moiety, contributing to its potential biological activity and specificity in interactions with biological targets. The presence of the fluorine atom may enhance lipophilicity and influence the compound's pharmacokinetic properties. As a boronic acid, it can participate in Suzuki coupling reactions, making it valuable in the synthesis of complex organic molecules. Additionally, its structural features suggest potential applications in drug development, particularly in the design of inhibitors or modulators of biological pathways. The compound's solubility, stability, and reactivity can be influenced by the pH of the environment, which is a critical consideration in its practical applications. Overall, this compound exemplifies the intersection of organic chemistry and medicinal applications.
Formula:C13H11BFNO3
InChI:InChI=1/C13H11BFNO3/c15-11-6-1-2-7-12(11)16-13(17)9-4-3-5-10(8-9)14(18)19/h1-8,18-19H,(H,16,17)
InChI key:InChIKey=WNFWVITXDBHCTD-UHFFFAOYSA-N
SMILES:C(NC1=C(F)C=CC=C1)(=O)C2=CC(B(O)O)=CC=C2
Synonyms:
  • B-[3-[[(2-Fluorophenyl)amino]carbonyl]phenyl]boronic acid
  • Boronic acid, B-[3-[[(2-fluorophenyl)amino]carbonyl]phenyl]-
  • Boronic acid, [3-[[(2-fluorophenyl)amino]carbonyl]phenyl]-
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