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CAS 850567-36-1

:

B-[3-[[(4-Cyanophenyl)amino]carbonyl]phenyl]boronic acid

Description:
B-[3-[[(4-Cyanophenyl)amino]carbonyl]phenyl]boronic acid, identified by its CAS number 850567-36-1, 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 organic synthesis and medicinal chemistry. The presence of the cyanophenyl group suggests potential electronic and steric effects that could influence its reactivity and solubility. Additionally, boronic acids are known for their role in Suzuki coupling reactions, which are pivotal in the formation of carbon-carbon bonds in organic synthesis. The compound may also exhibit biological activity, potentially serving as a pharmacophore in drug development. Its solubility and stability in different solvents can vary, impacting its utility in various chemical processes. Overall, this compound represents a versatile building block in both synthetic and medicinal chemistry.
Formula:C14H11BN2O3
InChI:InChI=1S/C14H11BN2O3/c16-9-10-4-6-13(7-5-10)17-14(18)11-2-1-3-12(8-11)15(19)20/h1-8,19-20H,(H,17,18)
InChI key:InChIKey=WDWVOWXKMQNJOX-UHFFFAOYSA-N
SMILES:C(NC1=CC=C(C#N)C=C1)(=O)C2=CC(B(O)O)=CC=C2
Synonyms:
  • Boronic acid, [3-[[(4-cyanophenyl)amino]carbonyl]phenyl]-
  • B-[3-[[(4-Cyanophenyl)amino]carbonyl]phenyl]boronic acid
  • Boronic acid, B-[3-[[(4-cyanophenyl)amino]carbonyl]phenyl]-
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