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CAS 1086111-17-2

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1H-Pyrazole-3-boronic acid pinacol ester

Description:
1H-Pyrazole-3-boronic acid pinacol ester is an organoboron compound characterized by the presence of a pyrazole ring and a boronic acid functional group, which is esterified with pinacol. This compound typically exhibits properties associated with both boron and nitrogen-containing heterocycles, making it useful in various chemical applications, particularly in organic synthesis and medicinal chemistry. The boronic acid moiety allows for participation in Suzuki-Miyaura cross-coupling reactions, facilitating the formation of carbon-carbon bonds. Additionally, the pyrazole ring contributes to the compound's potential biological activity, as pyrazole derivatives are often explored for their pharmacological properties. The pinacol ester enhances the stability and solubility of the boronic acid, making it easier to handle in laboratory settings. Overall, 1H-Pyrazole-3-boronic acid pinacol ester is a versatile compound with significant utility in synthetic organic chemistry and potential applications in drug development.
Formula:C9H15BN2O2
InChI:InChI=1/C9H15BN2O2/c1-8(2)9(3,4)14-10(13-8)7-5-6-11-12-7/h5-6H,1-4H3,(H,11,12)
SMILES:CC1(C)C(C)(C)OB(c2cc[nH]n2)O1
Synonyms:
  • 1H-pyrazole, 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
  • 1H-pyrazole, 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
  • 3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole
  • 5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole
  • 3-(4,4,5,5-Tetramethyl-1,3,2-Dioxabolone)-Pyrrazole
  • 3-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolane)-Pyrazole
  • Pyrazole-3-boronic acid pinacol ester
  • Pyrazole-5-boronic acid pinacol ester
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