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CAS 775351-40-1

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4-(1h-tetrazol-5-yl)benzene-1-boronic acid pinacol ester

Description:
4-(1H-tetrazol-5-yl)benzene-1-boronic acid pinacol ester is a chemical compound characterized by its boronic acid functionality, which is significant in various organic synthesis applications, particularly in Suzuki coupling reactions. This compound features a tetrazole ring, which contributes to its unique reactivity and potential biological activity. The pinacol ester moiety enhances its stability and solubility, making it suitable for various chemical transformations. Typically, boronic acids and their esters are known for their ability to form reversible complexes with diols, which can be exploited in sensor applications and drug delivery systems. The presence of the tetrazole group may also impart interesting pharmacological properties, as tetrazoles are often found in pharmaceuticals. Overall, this compound is of interest in both synthetic organic chemistry and medicinal chemistry due to its versatile reactivity and potential applications in drug development and materials science.
Formula:C13H17BN4O2
Synonyms:
  • 5-(4-Phenylboronic acid pinacol ester)-2H-tetrazole
  • 4-(2H-Tetrazol-5-yl)benzeneboronic acid pina
  • 4-(2H-TetrazoL
  • 4-(1H-Tetrazol-5-yl)benze...
  • 2H-Tetrazole, 5-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-
  • (4-(1h-tetrazol-5-yl)phenyl)boronic acid pinacol ester
  • 4-(1H-Tetrazol-5-yl)benzene-1-boronic acid pinacol ester
  • [4-(2H-tetrazol-5-yl)phenyl] boronic acid pinacol ester
  • 5-(4-(4,4,5,5-TetraMethyl-1,3,2-dioxaborolan-2-yl)phenyl)-2H-tetrazole
  • 5-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-2H-tetrazol
  • 4-(2H-Tetrazol-5-yl)benzeneboronic acid pinacol ester, 95%
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