CAS:1036378-83-2 | 2-([1,1':3',1''-terphenyl]-5'-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Introduction of CAS:1036378-83-2 | 2-([1,1':3',1''-terphenyl]-5'-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

4,4,5,5-Tetramethyl-2-[1,1':3',1''-terphenyl]-5'-yl-1,3,2-dioxaborolane (TMTD) is an organoboron compound that has a wide range of applications in scientific research. It is a versatile and powerful reagent that can be used in organic synthesis, biochemistry, and other areas of scientific research.

Specification of CAS:1036378-83-2 | 2-([1,1':3',1''-terphenyl]-5'-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Research Application of CAS:1036378-83-2 | 2-([1,1':3',1''-terphenyl]-5'-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Application in Synthesis of Boron-Containing Stilbenes

A series of 4,4,5,5-tetramethyl-2-(4-substitutedstyrylphenyl)-1,3,2-dioxaborolane derivatives were synthesized, leading to boron-containing stilbene derivatives. These compounds are used in the synthesis of boron-capped polyenes, which are potential intermediates for new materials in Liquid Crystal Display (LCD) technology. They are also being tested for potential therapeutic applications in neurodegenerative diseases (Das, Mahalingam, Das, Hosmane, & Evans, 2015).

Crystal Structure Analysis

The compound has been analyzed through crystal structure studies, providing detailed insights into its molecular structure. Such analyses are crucial for understanding the properties and potential applications of these compounds (Coombs, Vogels, Wheaton, Baerlocher, Baker, Decken, & Westcott, 2006).

Application in Nanoparticle Synthesis

The compound has been used in the synthesis of nanoparticles with enhanced brightness and emission tuning. These nanoparticles show great potential in applications such as bioimaging and sensing due to their high fluorescence quantum yields (Fischer, Baier, & Mecking, 2013).

Role in Synthesis of Novel Compounds

The compound is integral in the synthesis of novel compounds like mercapto- and piperazino-methyl-phenylboronic acid derivatives, which have been studied for their inhibitory activity against serine proteases (Spencer, Burd, Goodwin, Mérette, Scully, Adatia, & Deadman, 2002).

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