83871-65-2

Usage

Ethanediamine

Amino groups (-NH2) at both ends of the molecule

4-Methoxyphenyl

A phenyl ring with a methoxy group (-OCH3) attached to the 4th carbon

Phenyl

A phenyl ring (C6H5)

Molecular Weight

350.43 g/mol

Appearance

Unknown, but likely a solid or viscous liquid due to its molecular weight and structure

Solubility

Likely soluble in organic solvents such as ethanol, methanol, or acetone, due to its nonpolar phenyl and methoxyphenyl groups

Melting Point

Unknown, but expected to be relatively high due to the presence of multiple aromatic rings and potential for strong intermolecular interactions

Boiling Point

Unknown, but expected to be relatively high due to the molecular weight and complexity of the structure

Density

Unknown, but likely higher than water due to the presence of aromatic rings and the molecular weight

Pharmaceutical production

As a building block or intermediate in the synthesis of various drugs

Chelating agent

In chemical research and industrial processes, for binding and stabilizing metal ions

Coordination Complexes

Forms strong complexes with transition metal ions, useful in various chemical and biological applications

Anti-tumor properties

Under investigation for its potential to inhibit tumor growth

Anti-inflammatory properties

Being studied for its potential to reduce inflammation in the body

Medicinal Chemistry

A subject of interest in drug development due to its potential therapeutic properties and ability to form coordination complexes with metal ions

Upstream product

• 836-41-9 p-methoxybenzylidene-phenylamine 
• 1613-96-3 N-(4-methoxybenzylidene)aniline 
• 3585-93-1 N-(4-methoxybenzylidene)aniline oxide 

Downstream Products

• 1613-96-3 N-(4-methoxybenzylidene)aniline 

Relevant academic research and scientific papers

Reductive dimerization and reduction of imines using lanthanum metal

The treatment of N-benzylideneaniline (1a) with a half-equivalent of lanthanum metal and a catalytic amount of iodine gave the reductive dimerization product of 1a, a vic-diamine, in good yield. Various vic-diamines were synthesized from aldimines in this

A novel reductive dimerization/oxidative dehydrogenation of aldimines mediated by lanthanoid metals

A lanthanoid metal-mediated novel reductive dimerization/oxidative dehydrogenation of a variety of aldimines has been achieved. Aromatic aldimines (1) were dimerized in the presence of 0.5 mol of ytterbium metal (Yb) and 1-naphthaldehyde (1-NpCHO) to give

Indium-mediated deoxygenation of nitrones, N-oxides and deoxygenative reductive coupling of nitrones to vicinal diamines

We reported transformation of nitrones selectively either to aldamines or vicinal diamines and deoxygenation of N-oxides using Indium at ambient temperature in good yields.

Samarium diiodide/nickel diiodide an efficient system for homo and heterocoupling reactions of imines

Samarium diiodide in the presence of a catalytic amount of nickel diiodide mediates a very fast dimerization of imines into vicinal diamines and the mixed coupling of imines and ketones to give β-amino alcohols.

Reductive coupling of aldimines mediated with samarium catalyzed by Cp2TiCl2

Reductive coupling of aldimines into vicinal diamines mediated with samarium catalyzed by Cp2TiCl2 proceeds in refluxing THF with good yields.

Novel reductive coupling of aldimines to vicinal diamines

Reductive coupling of aldimines into vicinal diamines has been performed by the action of aluminium/bismuth powder and potassium hydroxide in methanol at ambient temperature in high yields.

Electrosynthesis of N-Substituted DL-Arylglycineesters and 1,2-Diarylamino-1,2-diarylethanes by Cathodic Reduction of Azomethines in the Presence of Carbon Dioxide

The electroreduction of the N-arylidene-arylamines 1-12 in CO2-saturated solvents of low proton availability as DMF at markedly more positive potentials than carbon dioxide end up in carboxylating the C-atom and hydrogenating the nitrogen of the C=N-double bond.The resulting N-arylsubstituted DL-arylglycines and traces of carbamates may be isolated as esters, adding ethylchloride during the electrolysis.A competing pathway of the electrocarboxylation is the C-C-hydrodimerisation and the hydrogenation of the C=N-double bond, whose importance increases with the water content of the solvent.Based on cyclic-voltametric evidence and product analysis the mechanism of the reductive electrocarboxylation reaction is discussed in terms of nucleophilic attack of the azomethine anion radical on a proton or CO2.