89114-75-0

Usage

Uses

Used in Pharmaceutical Industry:
N,N-Bis(4-methylphenyl)-4-(2-phenylethenyl)benzenamine is used as a building block for the synthesis of pharmaceuticals due to its unique structure and reactivity. It can contribute to the development of new drugs with specific therapeutic properties.
Used in Dye Industry:
In the dye industry, N,N-Bis(4-methylphenyl)-4-(2-phenylethenyl)benzenamine is used as a precursor in the production of various dyes. Its aromatic amine structure allows for the creation of dyes with distinct color characteristics and stability.
Used in Polymer Industry:
N,N-Bis(4-methylphenyl)-4-(2-phenylethenyl)benzenamine is also utilized in the polymer industry as a monomer or intermediate in the synthesis of polymers with specific properties. Its incorporation can lead to the development of polymers with tailored characteristics for various applications.
It is important to handle and use N,N-Bis(4-methylphenyl)-4-(2-phenylethenyl)benzenamine with caution due to potential hazards and risks associated with its exposure. Proper safety measures should be implemented during its use in research and industrial settings.

Upstream product

• 42906-19-4 4-[N,N-di(p-tolyl)amino]benzaldehyde 
• 1449-46-3 benzyltriphenylphosphonium bromide 
• 591-50-4 iodobenzene 
• 624-31-7 4-tolyl iodide 
• 1520-21-4 4-vinyl benzylamine 
• 108-86-1 bromobenzene 
• 106-38-7 para-bromotoluene 
• 74065-48-8 4-methyl-N-p-tolyl-N-(4-vinylphenyl)benzenamine 
• 106-43-4 para-chlorotoluene 

Relevant academic research and scientific papers

Synthesis and characterization of triphenylamine modified azobenzene dyes

A series of triphenylamine modified azobenzenes were synthesized and studied theoretically and experimentally. D-A-D structures of these dyes were revealed with an intramolecular charge transfer (ICT) from both triphenylamine or indoline units (donor) to

Ambipolar organic semiconductors with cascades of energy levels for generating long-lived charge separated states: A donor-acceptor1-acceptor2 architectural triarylamine dye

A donor-acceptor1-acceptor2 architectural 4-styryltriphenyl amine-based organic semiconductor was synthesized for solar cell applications. Sequential electron transfers together with effective hole transfer lead to a charge separated state lifetime of 650 ns, therefore boosting the short circuit current and efficiency of single layer organic photovoltaic cells. This journal is the Partner Organisations 2014.

One pot sequential reactions and novel products produced thereby

A method for producing sequenced reaction products comprising performing, in one pot, a first reaction at a lower temperature followed by a second reaction at a higher temperature in the presence of a catalyst system comprising a proazahosphatrane in combination with a palladium compound is provided. In one embodiment, the first reaction is a double amination reaction and the second reaction is an arylation. Use of one pot and a single catalyst system for each set of sequential reactions is efficient and economical. Novel N,N-diarylaminostyrenes and N,N-diarylaminostilbenes are produced according to the methods described herein.

Pd2dba3/P(i-BuNCH2CH2) 3N: A highly efficient catalyst for the one-pot synthesis of trans-4-N,N-diarylaminostilbenes and N,N-diarylaminostyrenes

A Pd2dba3/P(i-BuNCH2CH2) 3N catalyzed one-pot synthesis of unsymmetrically substituted trans-4-N,N-diarylaminostilbenes and both symmetrically and unsymmetrically substituted N,N-diarylaminostyrene derivatives is reported. The procedure involves two or more palladium catalyzed sequential coupling reactions (an amination and an inter-molecular Heck reaction) in one-pot using the same catalyst system with two different aryl halides, including aryl chlorides and hetero aryl halides as the coupling partners.

Disazo triphenylamine compounds

A disazo compound, having the general formula, STR1 wherein Y represents a substituted or non-substituted cyclic hydrocarbon or substituted or non-substituted heterocycle; R represents hydrogen, substituted or non-substituted alkyl group, or substituted or non-substituted phenyl group; and Z represents a substituted or non-substituted cyclic hydrocarbon or heterocycle fused with phenyl nucleus.