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CAS 874290-64-9

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[4-(5-oxopyrazolidin-3-yl)phenyl]boronic acid

Description:
[4-(5-oxopyrazolidin-3-yl)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, making it useful in various chemical applications, including drug development and materials science. The compound features a phenyl ring substituted with a pyrazolidinone moiety, contributing to its unique reactivity and potential biological activity. The oxopyrazolidin structure suggests that it may exhibit specific interactions with biological targets, possibly influencing its pharmacological properties. Additionally, the boronic acid group can participate in Suzuki coupling reactions, making it valuable in synthetic organic chemistry for constructing complex molecules. Its solubility and stability in various solvents can vary, which is important for its application in different chemical environments. Overall, [4-(5-oxopyrazolidin-3-yl)phenyl]boronic acid represents a versatile compound with potential implications in medicinal chemistry and materials science.
Formula:C9H11BN2O3
InChI:InChI=1/C9H11BN2O3/c13-9-5-8(11-12-9)6-1-3-7(4-2-6)10(14)15/h1-4,8,11,14-15H,5H2,(H,12,13)
SMILES:c1cc(ccc1C1CC(=NN1)O)B(O)O
Synonyms:
  • boronic acid, B-[4-(5-oxo-3-pyrazolidinyl)phenyl]-
  • [4-(5-Oxopyrazolidin-3-yl)phenyl]boronic acid
  • 4-(5-Oxopyrazolidin-3-yl)benzeneboronicacid96%
  • 4-(5-OXOPYRAZOLIDIN-3-YL)BENZENEBORONIC ACID
  • 4-(5-Oxopyrazolidin-3-yl)benzeneboronic acid 96%
  • 4-(5-OXOPYRAZOLIDIN-3-YL)PHENYLBORONIC ACID
  • 5-(4-BORONOPHENYL)PYRAZOLIDIN-3-ONE
  • 4-(5-Oxo-3-pyrazolidinyl)benzeneboronic acid, 96%
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