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4-(Diphenylamino)phenylboronicacid CAS:201802-67-7

4-(Diphenylamino)phenylboronic acid is a chemical compound with the molecular formula C18H16BNO2. It consists of a boronic acid group attached to a phenyl ring substituted with a diphenylamino moiety. This compound is notable for its potential applications in organic synthesis, materials science, and medicinal chemistry due to its unique structure and reactivity.

 


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Application and Effect:

4-(Diphenylamino)phenylboronic acid serves diverse purposes across various scientific domains owing to its distinctive properties. In organic synthesis, it acts as a valuable building block for constructing complex organic molecules. Its boronic acid functionality enables it to participate in Suzuki coupling reactions, facilitating the formation of carbon-carbon bonds and the synthesis of various functionalized compounds. Additionally, its reactivity with diols and other oxygen-containing compounds makes it a versatile tool for the development of new materials and pharmaceutical intermediates. In the field of materials science, 4-(Diphenylamino)phenylboronic acid is utilized in the design and fabrication of organic semiconductors and optoelectronic materials. Its diphenylamino unit contributes to its electron-donating properties, making it suitable for applications in organic light-emitting diodes (OLEDs), organic field-effect transistors (OFETs), and other electronic devices. Furthermore, its boronic acid functionality allows for the modification of polymer matrices, enabling the development of functionalized materials with tailored properties such as enhanced conductivity and luminescence. Moreover, in medicinal chemistry, 4-(Diphenylamino)phenylboronic acid plays a significant role in the synthesis of potential drug candidates and pharmacophores. Its ability to form stable complexes with biological targets makes it an important tool for the design of novel therapeutic agents, particularly in the areas of oncology and neuropharmacology. Additionally, it is employed in the development of fluorescent sensors for detecting biomolecules and monitoring cellular processes, contributing to advancements in biological research and diagnostics. Furthermore, this compound finds applications in catalysis and metal-ion sensing, where its boronic acid moiety enables selective recognition and binding of specific substrates and analytes. Its utility in diverse fields, including organic synthesis, materials science, medicinal chemistry, and chemical sensing, underscores its significance as a multifaceted compound with broad-reaching implications for scientific and technological advancement.

Product Sample:

Amino acid powder1
Amino acid powder2

Product Packing:

Amino acid powder3
Amino acid powder4
Amino acid powder5
Amino acid powder6

Additional Information:

Composition C18H16BNO2
Assay 99%
Appearance white powder
CAS No.  201802-67-7
Packing Small and bulk
Shelf Life 2 years
Storage Store in cool and dry area
Certification ISO.

 


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