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CAS 957061-02-8

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B-[4-(1H-Pyrazol-1-ylsulfonyl)phenyl]boronic acid

Description:
B-[4-(1H-Pyrazol-1-ylsulfonyl)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 and other nucleophiles. This compound features a phenyl ring substituted with a pyrazole moiety linked through a sulfonyl group, contributing to its unique reactivity and potential applications in medicinal chemistry, particularly in drug development and synthesis. The boronic acid group allows for participation in Suzuki coupling reactions, making it valuable in the synthesis of complex organic molecules. Additionally, the presence of the pyrazole and sulfonyl groups may impart specific biological activities, enhancing its utility in pharmaceutical applications. The compound is typically solid at room temperature and may exhibit solubility in polar organic solvents. Its properties, such as melting point, solubility, and reactivity, can vary based on environmental conditions and the presence of other functional groups in a reaction mixture. Overall, this compound represents a versatile building block in organic synthesis and medicinal chemistry.
Formula:C9H9BN2O4S
InChI:InChI=1S/C9H9BN2O4S/c13-10(14)8-2-4-9(5-3-8)17(15,16)12-7-1-6-11-12/h1-7,13-14H
InChI key:InChIKey=JEIPACYLLOVWOL-UHFFFAOYSA-N
SMILES:S(=O)(=O)(C1=CC=C(B(O)O)C=C1)N2C=CC=N2
Synonyms:
  • (4-((1H-Pyrazol-1-yl)sulfonyl)phenyl)boronic acid
  • Boronic acid, B-[4-(1H-pyrazol-1-ylsulfonyl)phenyl]-
  • (4-((1H-Pyrazol-1-yl)sulfonyl)phenyl)boronicacid
  • B-[4-(1H-Pyrazol-1-ylsulfonyl)phenyl]boronic acid
  • [4-(1H-Pyrazole-1-sulfonyl)phenyl]boronic acid
  • 4-(1H-Pyrazol-1-ylsulphonyl)benzeneboronicacid98%
  • 4-(1H-Pyrazol-1-ylsulfonyl)benzeneboronic acid, 98%
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