259197-87-0

Upstream product

• 5345-05-1 4-t-butyl-2,6-dimethylbromobenzene 
• 67-56-1 methanol 
• 64395-03-5 2-bromo-5-tert-butyl-isophthalic acid 

Downstream Products

• 522739-65-7 5-tert-butyl-2-(naphthalen-1-ylphenylamino)isophthalic acid dimethyl ester 
• 522739-70-4 5-tert-butyl-2-(dinaphthalen-1-ylamino)isophthalic acid dimethyl ester 
• 1338369-99-5 C₃₀H₂₆N₂O₂Se 
• 1338369-98-4 C₁₈H₁₆O₄Se 
• 1338370-04-9 C₃₀H₂₈N₂O₂Se 
• 1338370-02-7 C₁₈H₂₂O₂Se 

Relevant academic research and scientific papers

The substituent effect of bridged triarylamine helicenes on light-emitting and charge transfer properties

Methoxy-(7a), bromo-(7b), CF3-(7c) and hydroxyl-(7d) substituted bridged triarylamine helicenes were synthesized under mild conditions in 6598% yield. Their luminescence red-shifted with π-donating substituents and blue-shifted with the electro

Heterocyclic compounds and organic light-emitting diode including the same

The present invention relates to a heterocyclic compound represented by [Chemical Formula 1] below and an organic light-emitting diode including the same. The organic light-emitting diode according to the present invention is excellent in view of luminous characteristics such as driving voltage, lifespan, and efficiency. [Chemical Formula 1].

Aromatic ring strain in arylselenenyl bromides: Role in facile synthesis of selenenate esters via intramolecular cyclization

The synthesis and reactivity of 2,6-disubstituted arylselenium compounds derived from 2-bromo-5-tertbutylisophthalic acid (43) are described. The syntheses of bis(5-tert-butylisophthalic acid dimethyl ester)diselenide (46) and bis(5-tert-butylisophthalic

Bridged triarylamines: A new class of heterohelicenes

A series of bridged triarylamines, which constitute a new class of heterohelicenes, have been synthesized using a simple three-step procedure. These compounds are shown to be highly luminescent chromophores and are capable of being oxidized. The solid-sta

Formation and rearrangement of dithioxo- and diselenoxophosphoranes carrying bulky 4-t-butyl-2,6-bis(methoxyalkyl)phenyl groups

[4-t-Butyl-2,6-bis(1-methoxy-1-methylethyl)phenyl]phosphine, [4-t-butyl- 2,6-bis(2-methoxy-1,1-dimethylethyl)phenyl]phosphine, and [4-t-butyl-2,6- bis(3-methoxy-1,1-dimethylpropyl)phenyl]phosphine were prepared and allowed to react with sulfur or selenium, to give heterocyclic compounds containing phosphorus-oxygen bond, via rearrangement of the methyl moiety of the methoxy group.