3169-73-1

Basic information

• Product Name: 2-[4-(TERT-BUTYL)PHENOXY]ANILINE
• Synonyms: 2-[4-(TERT-BUTYL)PHENOXY]ANILINE;O-(P-TERT-BUTYLPHENOXY)-ANILINE
• CAS NO: 3169-73-1
• Molecular Formula: C₁₆H₁₉NO
• Molecular Weight: 241.33
• Mol File: 3169-73-1.mol
• Article Data: 3

Chemical Properties

• Melting Point: 83-84 °C
• Boiling Point: 339.4 °C at 760 mmHg
• Flash Point: 148.9 °C
• Appearance: /
• Density: 1.053 g/cm³
• PKA: 4.08±0.10(Predicted)
• CAS DataBase Reference: 2-[4-(TERT-BUTYL)PHENOXY]ANILINE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-[4-(TERT-BUTYL)PHENOXY]ANILINE(3169-73-1)
• EPA Substance Registry System: 2-[4-(TERT-BUTYL)PHENOXY]ANILINE(3169-73-1)

Safety Data

• Hazard Codes: Xi
• HazardClass: IRRITANT
• Hazardous Substances Data: 3169-73-1(Hazardous Substances Data)

Usage

General Description

2-[4-(tert-butyl)phenoxy]aniline is a chemical compound with the molecular formula C16H21NO. It is a synthetic compound often used in various industrial and research applications. The compound consists of a central aniline group attached to a phenoxy group, which in turn is linked to a tert-butyl group. 2-[4-(TERT-BUTYL)PHENOXY]ANILINE is often used as a building block in the synthesis of various organic molecules and polymers. It may also be used in the production of dyes, pigments, and other chemical products. 2-[4-(tert-butyl)phenoxy]aniline is generally considered to be a stable compound, but it should be handled with care and in accordance with proper safety protocols due to its potential hazards.

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 articles and documents

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

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.