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CAS 1029715-63-6

:

1-[3-(Tetrahydrofuryl)-1H-pyrazole-4-boronic acid pinacol ester

Description:
1-[3-(Tetrahydrofuryl)-1H-pyrazole-4-boronic acid pinacol ester, identified by its CAS number 1029715-63-6, is a boronic acid derivative characterized by the presence of a pyrazole ring and a tetrahydrofuryl 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. The pinacol ester functionality enhances its stability and solubility in organic solvents. Additionally, the presence of the tetrahydrofuryl moiety may contribute to its overall hydrophobic character, influencing its reactivity and interaction with other chemical species. This compound is of interest in medicinal chemistry and materials science due to its potential applications in drug development and as a building block in complex organic molecules. As with many boronic acids, it may also exhibit unique reactivity patterns in the presence of specific functional groups, making it a versatile intermediate in synthetic chemistry.
Formula:C13H21BN2O3
Synonyms:
  • 1-Tetrahydrofuran-3-yl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrazole
  • 1-(oxolan-3-yl)-4-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole
  • 1-(3-Tetrahydrofuryl)-1H-Pyrazole-4-Boronic Acid Pinacol Ester
  • 1-(oxolan-3-yl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrazole
  • 1-Tetrahydrofuran-3-yl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrazol
  • 1-(tetrahydrofuran-3-yl)-4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole
  • 1H-Pyrazole, 1-(tetrahydro-3-furanyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
  • 1-(3-Tetrahydrofuryl)-1H-...
  • 1-(Oxolan-3-yl)-4-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole 95+%
  • 1-(Oxolan-3-yl)-1H-pyrazole-4-boronic acid pinacol ester
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