1020-54-8

Basic information

• Product Name: Phenyl(4-ethoxyphenyl)amine
• Synonyms: 4-Ethoxy-N-phenylbenzenamine;Phenyl(4-ethoxyphenyl)amine
• CAS NO: 1020-54-8
• Molecular Formula: C₁₄H₁₅NO
• Molecular Weight: 213.275
• Mol File: 1020-54-8.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 349.5°Cat760mmHg
• Flash Point: 141.8°C
• Appearance: /
• Density: 1.088g/cm³
• Vapor Pressure: 4.68E-05mmHg at 25°C
• Refractive Index: 1.598
• CAS DataBase Reference: Phenyl(4-ethoxyphenyl)amine(CAS DataBase Reference)
• NIST Chemistry Reference: Phenyl(4-ethoxyphenyl)amine(1020-54-8)
• EPA Substance Registry System: Phenyl(4-ethoxyphenyl)amine(1020-54-8)

Safety Data

• Hazardous Substances Data: 1020-54-8(Hazardous Substances Data)

Usage

InChI:InChI=1/C14H15NO/c1-2-16-14-10-8-13(9-11-14)15-12-6-4-3-5-7-12/h3-11,15H,2H2,1H3

Upstream product

• 75-03-6 ethyl iodide 
• 122-37-2 4-anilinophenol 
• 64-67-5 diethyl sulfate 
• 156-43-4 4-Ethoxyaniline 
• 64-17-5 ethanol 
• 74-96-4 ethyl bromide 
• 108-90-7 chlorobenzene 
• 98-80-6 phenylboronic acid 
• 22237-13-4 (4-ethoxyphenyl)boronic acid 
• 143-66-8 sodium tetraphenyl borate 

Downstream Products

• 109533-97-3 (4-ethoxy-phenyl)-phenyl-carbamoyl chloride 
• 4316-52-3 4-ethoxytriphenylamine 
• 60457-49-0 N-(4-ethoxy-phenyl)-p-phenylenediamine 
• 7696-67-5 4'-Nitroso-4-aethoxy-diphenylamin 
• 38803-10-0 N,N'-bis-(4-phenetidino-phenyl)-thiourea 
• 94999-48-1 (4-ethoxy-phenyl)-phenyl-carbamic acid-(2-diethylamino-ethyl ester) 
• 675583-37-6 N,N'-diphenyl-N,N'-bis(4-ethoxyphenyl)-(9,9'-bianthracene)-10,10'-diamine 

Relevant articles and documents

Photogenerated diarylnitrenium ions: Laser flash photolysis and product studies on diphenylnitrenium ion generated from photolysis of 1-(N,N-diphenylamino)pyridinium ions

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Copper immobilized at a covalent organic framework: An efficient and recyclable heterogeneous catalyst for the Chan-Lam coupling reaction of aryl boronic acids and amines

A polyimide covalent organic framework (PI-COF) with high thermal and chemical stabilities has been readily prepared from commercially available and inexpensive reagents and was employed as an effective support for heterogeneous copper. It was demonstrated that the obtained Cu@PI-COF is a highly active heterogeneous catalyst which can effectively promote the Chan-Lam coupling reaction of aryl boronic acids and amines in an open flask without the aid of any base or additive. In addition, the catalyst could be readily recovered from the reaction mixture by simple filtration and reused for at least eight cycles without any observable change in structure and catalytic activity.

Solvent-free N-arylation of amines with arylboronic acids under ball milling conditions

Solvent-free coupling reactions of arylboronic acids with various amines were presented under ball milling conditions, achieving the aromatic amine coupling products with yields ranging from moderate to good. This type of mechano-chemistry exhibited advantages of solvent-free property, high efficiency, simple work-up procedure and eco-friendliness. This journal is the Partner Organisations 2014.