7249-78-7

Basic information

• Product Name: 2-(2-[2-(2-AMINOPHENOXY)ETHOXY]ETHOXY)ANILINE
• Synonyms: 2-(2-[2-(2-AMINOPHENOXY)ETHOXY]ETHOXY)ANILINE
• CAS NO: 7249-78-7
• Molecular Formula: C₁₆H₂₀N₂O₃
• Molecular Weight: 288.3416
• Mol File: 7249-78-7.mol
• Article Data: 17

Chemical Properties

• Melting Point: 65-66 °C
• Boiling Point: 494°Cat760mmHg
• Flash Point: 275.9°C
• Appearance: /
• Density: 1.19g/cm³
• Vapor Pressure: 6.69E-10mmHg at 25°C
• Refractive Index: 1.603
• PKA: 4.59±0.10(Predicted)
• CAS DataBase Reference: 2-(2-[2-(2-AMINOPHENOXY)ETHOXY]ETHOXY)ANILINE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2-[2-(2-AMINOPHENOXY)ETHOXY]ETHOXY)ANILINE(7249-78-7)
• EPA Substance Registry System: 2-(2-[2-(2-AMINOPHENOXY)ETHOXY]ETHOXY)ANILINE(7249-78-7)

Safety Data

• Hazardous Substances Data: 7249-78-7(Hazardous Substances Data)

Usage

Structure

Aniline derivative containing three ethylene glycol ether chains

Industrial applications

Corrosion inhibitor, surfactant, production of functional polymers

Usage

Intermediate in the synthesis of other compounds

Variation in properties and uses

Depends on the specific application

InChI:InChI=1/C16H20N2O3/c17-13-5-1-3-7-15(13)20-11-9-19-10-12-21-16-8-4-2-6-14(16)18/h1-8H,9-12,17-18H2

Upstream product

• 88-75-5 2-hydroxynitrobenzene 
• 100-52-7 benzaldehyde 
• 57-13-6 urea 
• 88-73-3 2-Chloronitrobenzene 
• 614-80-2 2-(acetylamino)phenol 
• 95-55-6 2-amino-phenol 
• 73776-05-3 bis-[2-(2-acetylamino-phenoxy)-ethyl] ether 
• 824-39-5 sodium o-nitrophenate 
• 111-44-4 3-oxa-1,5-dichloropentane 
• 54533-65-2 1,5-bis(o-nitrophenoxy)-3-oxapentane 

Downstream Products

• 120367-87-5 19-(Toluene-4-sulfonyl)-6,7,9,10,19,20-hexahydro-16H,18H,22H-5,8,11-trioxa-16,19,22-triaza-dibenzo[a,j]cyclooctadecene-17,21-dione 
• 126312-53-6 15,16,18,19-tetrahydro-7-phenyl-5H-dibenzo<1,11,14,4,5,7,8>trioxatetraazacyclohexadecyne 
• 1450928-54-7 C₅₂H₄₆N₂O₃P₂ 
• 1401622-90-9 C₂₂H₁₈N₈O₃ 
• 1401622-94-3 C₂₂H₂₀N₁₄O₃ 
• 1329608-97-0 C₃₀H₂₆Cl₂N₂O₅ 
• 86043-63-2 3,13-bis(4-nitrophenylazo)-6,7,9,10,16,17,18,19-octahydrodibenzo<1,4,7,10,13>trioxadiazacyclopentadecene 
• 109888-80-4 19-(Toluene-4-sulfonyl)-6,7,9,10,17,18,19,20,21,22-decahydro-16H-5,8,11-trioxa-16,19,22-triaza-dibenzo[a,j]cyclooctadecene 
• 144221-07-8 C₆H₂(CN)2CH₂N(SO₂C₆H₄CH₃)C₆H₄OC₂H₄OC₂H₄OC₆H₄N(SO₂C₆H₄CH₃)CH₂ 
• 144221-06-7 C₆H₂Br₂CH₂N(SO₂C₆H₄CH₃)C₆H₄OC₂H₄OC₂H₄OC₆H₄N(SO₂C₆H₄CH₃)CH₂ 

Relevant articles and documents

Diaryl-substituted polyethers with acetoacet-anilide fragment in the synthesis of dihydro-pyrimidine-containing podands

The interaction of ortho-aminoaryl polyethers, derivatives of mono-, di-, and triethylene glycol, with acetyl ketene, generated from 2,2,6-trimethyl-4H-1,3-dioxin-4-one produced acetoacetanilide- containing podands. 2,2,6-Trimethyl-4H-1,3-dioxin-4-one reacted with aminoaryl-substituted podands containing a short polyether chain (1-2 atoms) in toluene medium without catalyst. Acetoacetanilide- containing podands with longer polyether chains could be obtained by using triethylamine or acetic acid as catalyst. Acetoacetanilide-containing podands were used in the Biginelli reaction as CH-active components.

Fluorescent ion indicators for cadmium and lanthanide ion detection

The present invention provides a metal chelator and methods that facilitate binding, detecting, monitoring and quantitating of heavy metal ions in a sample. This metal chelating moiety has the following formula

Synthesis, characterization, tautomerism and theoretical study of some new Schiff base derivatives

New Schiff base derivatives were prepared by the condensation of 5-chloro and 5-bromo salicylaldehyde with bis(o-aminophenol)ethers. Five bis(o-nitrophenol)ether compounds were synthesized using some ditosylate, 1,3-dibromopropane and 1,4-dibromobuthane w