5487-93-4

Usage

Uses

Used in Organic Synthesis:
4,4'-BIPHENYLDIBORONIC ACID BIS(NEOPENTYL GLYCOL) ESTER is used as a building block in organic synthesis for the preparation of various types of organic compounds. Its unique structure and reactivity make it a valuable component in the synthesis of complex organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4,4'-BIPHENYLDIBORONIC ACID BIS(NEOPENTYL GLYCOL) ESTER is used as a precursor for the synthesis of boronic acid derivatives. These derivatives have potential applications in the development of new drugs and therapeutic agents, as they can be incorporated into the molecular structures of pharmaceutical compounds to enhance their properties and effectiveness.
Used in Material Science:
4,4'-BIPHENYLDIBORONIC ACID BIS(NEOPENTYL GLYCOL) ESTER is also utilized in material science for the synthesis of boronic acid derivatives that can be incorporated into the development of new materials with unique properties. These materials can be used in various applications, such as sensors, catalysts, and advanced materials for electronics and energy storage.
Used in Cross-Coupling Reactions:
4,4'-BIPHENYLDIBORONIC ACID BIS(NEOPENTYL GLYCOL) ESTER is used as a reactant in cross-coupling reactions, which are essential in the formation of carbon-carbon and carbon-heteroatom bonds in organic synthesis. These reactions play a crucial role in the synthesis of complex organic molecules and the development of new compounds with specific properties and applications.

Upstream product

• 624-38-4 para-diiodobenzene 
• 92-86-4 4-(4-bromophenyl)bromobenzene 
• 126-30-7 2,2-Dimethyl-1,3-propanediol 
• 4151-80-8 4,4'-biphenyldiboronic acid 

Downstream Products

• 4433-13-0 4,4'-divinyl-biphenyl 
• 4151-80-8 4,4'-biphenyldiboronic acid 
• 1417418-21-3 (4'-(5,5-dimethyl-1,3,2-dioxaborinan-2-yl)-[1,1'-biphenyl]-4-yl)(phenyl)iodonium trifluoroacetate 
• 612480-23-6 4,4'-bis(2',2,6',6-tetracarboxy-4,4':4',4-pyridyl)-1,1-biphenyl 
• 25627-15-0 1,4'''-dinitro-4,1':4',1'':4'',1'''-quaterphenylene 
• 117878-74-7 1,4'''-di-N,N-dimethylamino-4,1':4',1'':4'',1'''-quaterphenylene 

Relevant academic research and scientific papers

Size-controlled synthesis of conjugated polymer nanoparticles in confined nanoreactors

Soluble conjugated polymeric nanoparticles are synthesized by Suzuki-type polycondensation of two monomers (Ax + By, x>2, y≥2) in the channel of ordered mesoporous silica-supported carbon nano-membranes (nanoreactors). These synthesized soluble conjugated microporous polymers (SCMPs) exhibit uniform particle-size distributions and well-controlled particle sizes. The control of particle size stems from the fact that the polycondensations exclusively take place inside the mesochannels of the nano-reactors. Photo-luminescence studies show that polymeric nanoparticles with tetraphenylethene and pyrene substructures are highly fluorescent. The combination of both physical stability and process-ability offered by the soluble polymeric nanoparticles makes them particularly attractive in light emitting and other optoelectronic applications.