Introduction of CAS:219488-97-8 | 4,4,5,5-tetramethyl-2-(1,2,2-triphenylvinyl)-1,3,2-dioxaborolane
2-(alpha,beta-Diphenylstyryl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, also known as DBTMD, is a boronic acid derivative that has been studied extensively for its potential applications in a variety of scientific research fields.
Specification of CAS:219488-97-8 | 4,4,5,5-tetramethyl-2-(1,2,2-triphenylvinyl)-1,3,2-dioxaborolane
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ITEMS |
SPECIFICATION |
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Density |
1.09±0.1 g/cm3(Predicted) |
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Boiling Point |
441.1±55.0 °C(Predicted) |
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Molecular Formula |
C26H27BO2 |
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Molecular Weight |
382.3 |
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Purity |
98% |
Research Application of CAS:219488-97-8 | 4,4,5,5-tetramethyl-2-(1,2,2-triphenylvinyl)-1,3,2-dioxaborolane
Electrochemical Properties and Reactions:Studies on 4,4,5,5-tetramethyl-2-phenylsulfanylmethyl-[1,3,2]dioxaborolane revealed its electrochemical properties. Comparative analyses indicated a much lower oxidation potential compared to organoborane, demonstrating unique electrochemical behavior that could have implications in various scientific applications (Tanigawa et al., 2016).
Synthesis of Vinylboronates:Research on the dehydrogenative borylation of vinylarenes using pinacolborane (4,4,5,5-tetramethyl-1,3,2-dioxaborolane) has been successful. This process allows the synthesis of regio- and stereodefined (E)-2-arylethenylboronates. The use of rhodium and ruthenium catalysts in this process highlights the compound's versatility in organic synthesis (Murata et al., 2002).
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