3169-73-1

Usage

Uses

Used in Organic Synthesis:
2-[4-(TERT-BUTYL)PHENOXY]ANILINE is used as a building block for the synthesis of various organic molecules and polymers, contributing to the structural diversity and functional properties of the resulting compounds.
Used in Chemical Product Production:
In the chemical industry, 2-[4-(TERT-BUTYL)PHENOXY]ANILINE is used in the production of dyes, pigments, and other chemical products, enhancing their color characteristics and performance in various applications.
Used in Research Applications:
2-[4-(TERT-BUTYL)PHENOXY]ANILINE also serves as a valuable reagent in research settings, where it can be employed to explore new chemical reactions, mechanisms, and the development of novel materials.
It is important to handle 2-[4-(TERT-BUTYL)PHENOXY]ANILINE with care and follow proper safety protocols due to its potential hazards, ensuring the safety of both individuals and the environment.

Upstream product

• 3169-72-0 1-(4-(tert-butyl)phenoxy)-2-nitrobenzene 
• 98-54-4 para-tert-butylphenol 
• 88-73-3 2-Chloronitrobenzene 
• 1493-27-2 ortho-nitrofluorobenzene 

Downstream Products

• 1527494-49-0 N-(2-bromo-4-fluorophenyl)-N-(3-(2-(4-tert-butylphenoxy)phenyl)prop-2-yn-1-yl)acetamide 
• 1527494-35-4 1-(4-(tert-butyl)phenoxy)-2-iodobenzene 

Relevant academic research and scientific papers

Distance-Dependent Attractive and Repulsive Interactions of Bulky Alkyl Groups

The stabilizing and destabilizing effects of alkyl groups on an aromatic stacking interaction were experimentally measured in solution. The size (Me, Et, iPr, and tBu) and position (meta and para) of the alkyl groups were varied in a molecular balance mod

Four- and Sixfold Tandem-Domino Reactions Leading to Dimeric Tetrasubstituted Alkenes Suitable as Molecular Switches

A highly efficient palladium-catalyzed fourfold tandem-domino reaction consisting of two carbopalladation and two C-H-activation steps was developed for the synthesis of two types of tetrasubstituted alkenes 3 and 6 with intrinsic helical chirality starting from substrates 1 and 4, respectively. A sixfold tandem-domino reaction was also developed by including a Sonogashira reaction. 20 compounds with different substitution patterns were prepared with yields of up to 97%. Structure elucidation by X-ray crystallography confirmed helical chirality of the two alkene moieties. Photophysical investigations of some of the compounds showed pronounced switching properties through light-controlled changes of their stereochemical configuration.

A Fast Way to Fluorescence: A Fourfold Domino Reaction to Condensed Polycyclic Compounds

A fast and efficient palladium-catalyzed fourfold domino Sonogashira/double-carbopalladation/C H-activation reaction that converts simple aromatic systems into complex polycyclic hydrocarbons has been developed. A number of substituted products has thus been prepared in yields up to 89 %. The structural assignment has been confirmed by using single-crystal X-ray crystallography. The products show intriguing fluorescence activity and thus might serve as chemical sensors or fluorescent imaging dyes.