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CAS 1040377-03-4

:

1-(Tetrahydro-2H-pyran-4-yl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole

Description:
1-(Tetrahydro-2H-pyran-4-yl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole, identified by CAS number 1040377-03-4, is a chemical compound characterized by its unique structural features, which include a pyrazole ring and a tetrahydropyran moiety. The presence of the dioxaborolane group suggests potential applications in organoboron chemistry, particularly in cross-coupling reactions and as a reagent in organic synthesis. This compound may exhibit interesting biological activities due to the pyrazole structure, which is often associated with pharmacological properties. Its solubility, stability, and reactivity can be influenced by the functional groups present, making it a candidate for various synthetic applications. Additionally, the steric hindrance introduced by the tetramethyl groups may affect its interaction with other molecules, potentially enhancing selectivity in chemical reactions. Overall, this compound represents a versatile building block in organic synthesis and medicinal chemistry, warranting further investigation into its properties and applications.
Formula:C14H23BN2O3
InChI:InChI=1S/C14H23BN2O3/c1-13(2)14(3,4)20-15(19-13)11-9-16-17(10-11)12-5-7-18-8-6-12/h9-10,12H,5-8H2,1-4H3
InChI key:InChIKey=BOOVIFJKQGYEON-UHFFFAOYSA-N
SMILES:CC1(C)OB(OC1(C)C)C2=CN(N=C2)C3CCOCC3
Synonyms:
  • 1-(Oxan-4-yl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrazole
  • 1-(Tetrahydro-pyran-4-yl)-1H-pyrazole-4-Boronic acid pinacol ester
  • 1-(Tetrahydropyran-4-yl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole
  • 1-(Tetrahydropyran-4-yl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrazole
  • 1-(oxan-4-yl)-4-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole
  • 1H-Pyrazole, 1-(tetrahydro-2H-pyran-4-yl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
  • 1-(Tetrahydro-2H-pyran-4-yl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole
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