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CAS 947533-31-5

:

(1-tert-butoxycarbonylpyrazol-4-yl)boronic acid

Description:
(1-tert-butoxycarbonylpyrazol-4-yl)boronic acid is a boronic acid derivative characterized by the presence of a pyrazole ring substituted with a tert-butoxycarbonyl (Boc) group. 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 organic synthesis applications, particularly in the formation of carbon-carbon bonds through Suzuki coupling reactions. The presence of the pyrazole moiety can impart unique reactivity and selectivity in chemical reactions, while the Boc group serves as a protective group that can be removed under acidic conditions, allowing for further functionalization of the molecule. Additionally, this compound may exhibit moderate solubility in organic solvents and can be sensitive to moisture, which is a common characteristic of boronic acids. Its applications may extend to medicinal chemistry, where it could serve as a building block for the synthesis of biologically active compounds.
Formula:C8H13BN2O4
InChI:InChI=1/C8H13BN2O4/c1-8(2,3)15-7(12)11-5-6(4-10-11)9(13)14/h4-5,13-14H,1-3H3
SMILES:CC(C)(C)OC(=O)n1cc(cn1)B(O)O
Synonyms:
  • 1-tert-Butoxycarbonyl-1H-pyrazole-4-boronic acid
  • [1-(tert-Butoxycarbonyl)-1H-pyrazol-4-yl]boronic acid
  • 1-(tert-Butoxycarbonyl)pyrazole-4-boronicacid
  • 1-Boc-1H-Pyrazole-4-Boronic Acid
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