782504-35-2

Usage

Uses

Due to the limited information available on 4-T-butyl-N-(4-isopropylphenyl)benzenamine, its specific applications are not well-defined. However, given its classification as a triarylamine, it may potentially be used in various industries, such as:
Used in Chemical Industry:
4-T-butyl-N-(4-isopropylphenyl)benzenamine could be used as a chemical intermediate for the synthesis of more complex organic compounds or as a component in the development of new materials.
Used in Pharmaceutical Industry:
As a triarylamine, 4-T-butyl-N-(4-isopropylphenyl)benzenamine might be explored for its potential pharmaceutical applications, such as in the development of new drugs or as a building block for drug molecules.
Used in Research and Development:
4-T-butyl-N-(4-isopropylphenyl)benzenamine could be utilized in academic or industrial research settings to study its properties, reactivity, and potential applications in various fields.
It is crucial to note that any potential usage of 4-T-butyl-N-(4-isopropylphenyl)benzenamine should be supported by thorough research and safety checks, and appropriate personal protective equipment should be worn when handling this chemical compound.

Upstream product

• 3972-65-4 1-bromo-4-tert-butylbenzene 
• 99-88-7 4-Isopropylaniline 
• 5433-01-2 1-bromo-3-isopropylbenzene 
• 5369-19-7 3-tert-butylaniline 

Downstream Products

• 1044870-00-9 4-bromo-N-(4-t-butylphenyl)-N-(4-isopropylphenyl)benzenamine 
• 1174040-32-4 C₇₄H₈₈N₂ 
• 1268515-15-6 C₇₆H₇₀N₂O₂ 

Relevant academic research and scientific papers

New compounds and organic light-emitting diode including the same

PURPOSE: A fused aryl compound is provided to be stable and to have excellent luminous efficiency, thereby capable of providing an organic electroluminescence device with excellent driving voltage, external quantum efficiency, color purity and life time performance. CONSTITUTION: A fused aryl compound is represented by chemical formula 1. In chemical formula 1, each of R is selected from hydrogen, deuterium, substituted or unsubstituted C1-6 alkyl, substituted or unsubstituted C7-30, substituted or unsubstituted C3-30 cycloalkyl, substituted or unsubstituted C5-30 cycloalkenyl, substituted or unsubstituted C1-30 alkoxy, substituted or unsubstituted C6-30 aryloxy, substituted or unsubstituted C1-30 alkylthioxy, substituted or unsubstituted C5-30 arylthioxy, substituted or unsubstituted C1-30 alkylamine, substituted or unsubstituted C5-30 arylamine, substituted or unsubstituted C5-50 aryl, substituted or unsubstituted heteroaryl, substituted or unsubstituted silicon, substituted or unsubstituted boron, substituted or unsubstituted silane, carbonyl, phosphoryl, amino, nitrile, hydroxy, nitro, halogen, amide, and ester.

AROMATIC AMINE DERIVATIVES AND ORGANIC LIGHT EMITTING LAYER AND DIODE COMPRISING THE SAME

Disclosed are aromatic amine derivatives that can significantly improve material lifetime and luminous efficiency by introducing substituted or unsubstituted, saturated or unsaturated, hexagonal or more polygonal hydrocarbon rings into positions 2, 3, 6 a