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CAS 957034-65-0

:

B-[3-Chloro-4-[(cyclohexylamino)carbonyl]phenyl]boronic acid

Description:
B-[3-Chloro-4-[(cyclohexylamino)carbonyl]phenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The compound features a chlorinated phenyl ring, which can influence its reactivity and solubility, as well as a cyclohexylamino carbonyl substituent that may enhance its biological activity or selectivity in target interactions. The boronic acid moiety allows for participation in Suzuki coupling reactions, a key method for forming carbon-carbon bonds in organic synthesis. Additionally, the presence of the cyclohexyl group may contribute to the compound's lipophilicity, potentially affecting its pharmacokinetic properties. Overall, this compound's unique structural features make it a valuable candidate for research in drug development and materials science, particularly in the context of targeted therapies and advanced synthetic methodologies.
Formula:C13H17BClNO3
InChI:InChI=1S/C13H17BClNO3/c15-12-8-9(14(18)19)6-7-11(12)13(17)16-10-4-2-1-3-5-10/h6-8,10,18-19H,1-5H2,(H,16,17)
InChI key:InChIKey=MRKODTKFSLUDTB-UHFFFAOYSA-N
SMILES:C(NC1CCCCC1)(=O)C2=C(Cl)C=C(B(O)O)C=C2
Synonyms:
  • (3-Chloro-4-(cyclohexylcarbamoyl)phenyl)boronic acid
  • (3-Chloro-4-(cyclohexylcarbamoyl)phenyl)boronicacid
  • 3-Chloro-4-(cyclohexylcarbamoyl)benzeneboronic acid
  • 3-Chloro-4-(cyclohexylcarbamoyl)phenylboronic acid
  • B-[3-Chloro-4-[(cyclohexylamino)carbonyl]phenyl]boronic acid
  • Boronic acid, B-[3-chloro-4-[(cyclohexylamino)carbonyl]phenyl]-
  • 3-Chloro-4-(cyclohexylcarbamoyl)benzeneboronicacid96%
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