CAS:852475-03-7 | [4-(Triphenylsilyl)phenyl]boronic Acid

Introduction of CAS:852475-03-7 | [4-(Triphenylsilyl)phenyl]boronic acid

While the provided papers do not directly discuss (4-(Triphenylsilyl)phenyl)boronic acid, they offer insights into the broader category of boronic acids and their chemical behavior. Boronic acids, in general, are known for their versatility as building blocks in the construction of complex molecular architectures. They can be used to create macrocycles, cages, dendritic structures, rotaxanes, and polymers through reversible condensation reactions. The unique properties of boronic acids make them valuable in various chemical reactions and material science applications.

Specification of CAS:852475-03-7 | [4-(Triphenylsilyl)phenyl]boronic acid

Research Application of CAS:852475-03-7 | [4-(Triphenylsilyl)phenyl]boronic acid

Optical Modulation and Sensing

One significant application of phenyl boronic acids, including structures similar to (4-(Triphenylsilyl)phenyl)boronic acid, is their role in optical modulation and sensing. For instance, phenyl boronic acids have been utilized for saccharide recognition due to their binding affinity to pendant diols. This property has been harnessed in the development of sensor technologies, such as the aqueous dispersion of single-walled carbon nanotubes (SWNT), which quench near-infrared fluorescence in response to saccharide binding. This demonstrates a clear link between the molecular structure of phenyl boronic acids and the optical properties of SWNT, paving the way for advanced sensing applications (Mu et al., 2012).

Fluorescence Recognition in Biological Systems

Another application is in the development of fluorescent probes for biological systems. A new boronic acid derivative was synthesized for use as a sequential "on-off-on"-type relay fluorescence probe for Fe3+ ions and F- ions with high selectivity and sensitivity under physiological conditions. This innovation holds significant potential for applications in real water sample testing and bioimaging, particularly for detecting intracellular Fe3+ and F- in living cells, demonstrating the versatility of phenyl boronic acids in biological and environmental monitoring (Selvaraj et al., 2019).

Catalysis and Organic Synthesis

Phenyl boronic acids also find applications in catalysis and organic synthesis. For example, they have been used as catalysts for dehydrative amidation between carboxylic acids and amines, facilitating α-dipeptide synthesis. This highlights their role in accelerating organic synthesis processes through the catalytic activity of boronic acid derivatives (Wang et al., 2018).

Antiviral Therapeutics

Moreover, phenylboronic-acid-modified nanoparticles have shown promise as antiviral therapeutics. This novel application explores the potential of boronic acid functionalized nanoparticles as viral entry inhibitors, providing a new avenue for antiviral therapy development, especially against the Hepatitis C virus (Khanal et al., 2013).

Hot Tags: cas:852475-03-7 | [4-(triphenylsilyl)phenyl]boronic acid, China cas:852475-03-7 | [4-(triphenylsilyl)phenyl]boronic acid manufacturers, factory, Chemical Reagents, Methyltin mercaptide