4,4,5,5-tetramethyl-2-(1,2,2-triphenylvinyl)-1,3,2-dioxaborolane
98%
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description Product Description
This compound serves as a boronic ester reagent in carbon-carbon bond-forming reactions, particularly the Suzuki-Miyaura cross-coupling, which is widely used in organic synthesis to create complex structures such as bioactive molecules or organic materials for electronic devices. Owing to its triphenylvinyl moiety with luminescent properties, it is utilized in developing emissive materials, including organic light-emitting diodes (OLEDs) and sensors for specific analytes. It displays aggregation-induced emission (AIE), remaining non-emissive in dilute solutions but exhibiting strong fluorescence in aggregated or viscous states, making it an effective fluorescent probe for biological imaging applications like tracking cellular processes, monitoring membrane dynamics, and detecting microviscosity changes in live cells. Its stability and tunable emission further enable its use in sensor development for environmental and industrial monitoring.
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