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CAS 874288-01-4

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

Description:
B-[4-[[(2-Bromophenyl)amino]carbonyl]phenyl]boronic acid is an organic compound characterized by its boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, including medicinal chemistry and materials science. The compound features a boron atom bonded to a phenyl group and an amide linkage, which contributes to its potential as a building block in drug development and as a ligand in catalysis. The presence of the bromophenyl moiety enhances its reactivity and solubility in organic solvents. Additionally, boronic acids are often utilized in Suzuki coupling reactions, facilitating the formation of carbon-carbon bonds, which is crucial in synthesizing complex organic molecules. The compound's structure suggests it may exhibit specific biological activities, making it a candidate for further investigation in pharmaceutical research. Its unique properties stem from the interplay of its functional groups, which influence its reactivity, solubility, and potential applications in various chemical processes.
Formula:C13H11BBrNO3
InChI:InChI=1S/C13H11BBrNO3/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=COKKVGHDIYNFCQ-UHFFFAOYSA-N
SMILES:C(NC1=C(Br)C=CC=C1)(=O)C2=CC=C(B(O)O)C=C2
Synonyms:
  • Boronic acid, [4-[[(2-bromophenyl)amino]carbonyl]phenyl]-
  • B-[4-[[(2-Bromophenyl)amino]carbonyl]phenyl]boronic acid
  • Boronic acid, B-[4-[[(2-bromophenyl)amino]carbonyl]phenyl]-
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