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1-phenyl-2-(phenyl-4-boronicacid)-benzimidazole CAS:952514-79-3

1-phenyl-2-(phenyl-4-boronicacid)-benzimidazole, with the chemical formula C19H14B N2O2, is a compound containing a benzimidazole ring substituted with a phenyl group and a boronic acid moiety. This compound exhibits potential applications in organic synthesis, medicinal chemistry, and material science due to its unique structure and reactivity.

 


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Application and Effect:

1-phenyl-2-(phenyl-4-boronicacid)-benzimidazole offers diverse utility across various scientific disciplines owing to its distinctive properties. In organic synthesis, it serves as a valuable building block for constructing complex organic molecules. Its boronic acid functionality allows it to participate in Suzuki-Miyaura cross-coupling reactions, facilitating the formation of carbon-carbon bonds and the synthesis of diverse functionalized compounds. Additionally, its reactivity with diols and other oxygen-containing compounds makes it an invaluable tool for the development of new materials and pharmaceutical intermediates. In the field of medicinal chemistry, 1-phenyl-2-(phenyl-4-boronicacid)-benzimidazole plays a significant role in the design and synthesis of potential drug candidates. Its structural features make it suitable for interactions with biological targets, contributing to its application in drug discovery and development. The compound's pharmacological properties and potential therapeutic effects make it a subject of interest in pharmaceutical research aimed at addressing various diseases and medical conditions, including cancer, infectious diseases, and neurological disorders. Furthermore, this compound finds applications in material science, particularly in the design and synthesis of organic semiconductors and optoelectronic materials. Its structural components contribute to its electronic properties, making it suitable for use in organic light-emitting diodes (OLEDs), organic photovoltaic cells (OPVs), and other electronic devices. Moreover, its ability to interact with specific functional groups enables the modification of polymer matrices, leading to the development of functionalized materials with tailored properties such as enhanced conductivity and light-emission characteristics. Additionally, 1-phenyl-2-(phenyl-4-boronicacid)-benzimidazole may find utility in chemical sensing applications, where its boronic acid moiety enables selective recognition and binding of specific analytes. Its multifaceted properties and potential applications underscore its significance as a versatile compound with broad-reaching implications for scientific research and technological advancements in fields such as organic synthesis, medicinal chemistry, material science, and chemical sensing.

 

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 C19H14BN2O2
Assay 99%
Appearance white powder
CAS No.  952514-79-3
Packing Small and bulk
Shelf Life 2 years
Storage Store in cool and dry area
Certification ISO.

 


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