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CAS 349666-24-6

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Pyrenyl-1-boronic acid pinacol ester

Description:
Pyrenyl-1-boronic acid pinacol ester is an organoboron compound characterized by the presence of a pyrene moiety, which is a polycyclic aromatic hydrocarbon known for its fluorescence properties. This compound typically features a boronic acid functional group that is esterified with pinacol, enhancing its stability and solubility in organic solvents. The presence of the pyrene group imparts unique optical properties, making it useful in various applications, including organic electronics, sensors, and fluorescent probes. Pyrenyl-1-boronic acid pinacol ester can participate in Suzuki-Miyaura cross-coupling reactions, which are valuable in the synthesis of complex organic molecules. Additionally, its boronic acid functionality allows for reversible binding with diols, making it useful in biological applications and materials science. The compound is generally handled with standard safety precautions due to its potential reactivity and the presence of boron, which can be toxic in certain forms. Overall, its distinctive structural features and reactivity make it a significant compound in organic synthesis and materials research.
Formula:C22H21BO2
InChI:InChI=1/C22H21BO2/c1-21(2)22(3,4)25-23(24-21)18-13-11-16-9-8-14-6-5-7-15-10-12-17(18)20(16)19(14)15/h5-13H,1-4H3
Synonyms:
  • 4,4,5,5-Tetramethyl-2-(1-pyrenyl)-1,3,2-dioxaborolane
  • 4,4,5,5-tetramethyl-2-(pyren-1-yl)-1,3,2-dioxaborolane
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