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CAS 850568-27-3

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

Description:
B-[4-[[(4-Fluorophenyl)amino]carbonyl]phenyl]boronic acid, identified by its CAS number 850568-27-3, is a boronic acid derivative characterized by the presence of a boron atom bonded to a phenyl group and an amino carbonyl 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 drug development and organic synthesis. The presence of the fluorophenyl group may enhance its biological activity and solubility, while the amino carbonyl moiety can participate in hydrogen bonding and other interactions. This compound is likely to be a solid at room temperature and may be soluble in polar organic solvents. Its reactivity and functional groups suggest potential applications in medicinal chemistry, particularly in the design of inhibitors or modulators of biological targets. As with many boronic acids, it may also be involved in Suzuki coupling reactions, a key method in organic synthesis for forming carbon-carbon bonds.
Formula:C13H11BFNO3
InChI:InChI=1S/C13H11BFNO3/c15-11-5-7-12(8-6-11)16-13(17)9-1-3-10(4-2-9)14(18)19/h1-8,18-19H,(H,16,17)
InChI key:InChIKey=HIHZUEQBMMAFSA-UHFFFAOYSA-N
SMILES:C(NC1=CC=C(F)C=C1)(=O)C2=CC=C(B(O)O)C=C2
Synonyms:
  • B-[4-[[(4-Fluorophenyl)amino]carbonyl]phenyl]boronic acid
  • Boronic acid, B-[4-[[(4-fluorophenyl)amino]carbonyl]phenyl]-
  • [4-[(4-Fluorophenyl)carbamoyl]phenyl]boronic acid
  • Boronic acid, [4-[[(4-fluorophenyl)amino]carbonyl]phenyl]-
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