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Usage

Uses

Used in Coordination Chemistry:
N,N'-Bis(2'-aminophenyl)ethylene diamine is used as a ligand for forming stable complexes with metal ions, particularly transition metals. Its chelating properties are valuable in this application for enhancing the stability and reactivity of metal complexes.
Used in Catalysis:
In the field of catalysis, N,N'-Bis(2'-aminophenyl)ethylene diamine is utilized to create active catalysts by forming complexes with metal ions. These complexes can facilitate various chemical reactions, improving the efficiency and selectivity of catalytic processes.
Used in Separation Processes:
N,N'-Bis(2'-aminophenyl)ethylene diamine is employed in separation processes as a chelating agent to selectively bind and separate metal ions from complex mixtures, which is crucial in environmental remediation and industrial purification tasks.
Used in Synthesis of Organic Compounds and Materials:
N,N'-Bis(2'-aminophenyl)ethylene diamine is used as a building block in the synthesis of a variety of organic compounds and materials, contributing to the development of new chemical entities and materials with specific properties.
Used in Pharmaceutical Research:
In the pharmaceutical industry, N,N'-Bis(2'-aminophenyl)ethylene diamine is investigated for its potential antitumor and antituberculosis activities. Its ability to form complexes with metal ions is being explored for the development of new drugs targeting these diseases.
Each of these applications leverages the unique properties of N,N'-Bis(2'-aminophenyl)ethylene diamine, highlighting its versatility and importance in multiple scientific and industrial domains.

Upstream product

• 131543-46-9 Glyoxal 
• 95-54-5 1,2-diamino-benzene 
• 88-73-3 2-Chloronitrobenzene 
• 1493-27-2 ortho-nitrofluorobenzene 
• 5431-37-8 N,N’-bis(2-nitrophenyl)-1,2-ethanediamine 

Downstream Products

• 123885-72-3 2,2'-(ethane-1,2-diylbis(azanediyl)bis(2,1-phenylene)bis(azaneylylidene)bis(methaneylylidene))diphenol 
• 873550-34-6 1,4,7,10,13-pentaazacyclopentadecane 

Relevant academic research and scientific papers

Synthesis, characterization and X-ray structural determination of a stable dication derived from symmetrical ortho-aminophenyl diamine and 2-pyridinecarboxaldehyde

N,N′-Bis(2-aminophenyl)-1,2-ethanediamine is synthesized from 1,2-diaminoethane and 1-chloro-2-nitrobenzene in the presence of sodium carbonate and the product reduced by zinc dust and ammonium chloride. A novel stable dication is synthesized by reaction

Graphene-oxide/schiff base N2O4 ligand-palladium: A new catalyst for the synthesis of furan derivatives

In this paper, we aimed at synthesizing GO/H2L-Pd nano-composites (graphene-oxide/schiff base N2O4 Ligand-palladium) as a new heterogeneous catalyst. Different analytical techniques were applied in order to analyze the chemical composition and the structure of the catalyst. The findings revealed that GO/H2L-Pd could catalyze synthesis of furan derivatives in one-pot three-component condensation reaction by different aromatic aldehydes, arylamine and acetylenedicarboxylate. The major advantages of this study are the green and mild procedure, easy reaction work-up, short reaction time, high yields, and reusability of the catalyst.

Salicylimine-based fluorescent chemosensor for magnesium ions in aqueous solution

A new fluorescent schiff base chemosensor (H2L) was prepared for the sensitive and selective sensing of Mg2+ ions based on multiple mechanisms. H2L is a weak fluorescent (f = 0.031) due to PET process and C[dbnd]N isomeriz

Synthetic and structural investigations of bis(N -alkyl-benzoselenadiazolium) cations

The synthesis, and spectroscopic and structural characterization of bridged dicationic derivatives of benzo-2,1,3-selenadiazoles are reported. The chloride salt of [H4C6NSeN-CH2-CH2-NSeNC6H4/sub

Cu-catalyzed asymmetric conjugate addition of dialkylzincs to enones using a (±)- trans -1,2-cyclohexanediamine-based bis(NHC) derived from l -leucinol

A hydroxyamide-functionalized azolium salt as the precursor of a (±)-trans-1,2-cyclohexanediamine-based bis(NHC) ligand was designed and synthesized from readily accessible l-leucinol. The combination of a Cu salt with this chiral ligand precursor promote

Synthesis and Reactivity of Polyamines: Part 2 - Reactivity of Substrates with Terminal Aniline Units

The tetraamino compound (2) reacts with N,N'-bis-carbomethoxy-S-methylisothiourea to form the bisbenzimidazole (9).The secondary aliphatic amines in the link portion of the nitroanilines (3) and (5) could be protected by acylation.Subsequent reduction giv

Syntheses and Reactivity of Bisflavins. Oxidation of N-Benzyl-1,4-dihydronicotinamide by Flavins in Aqueous Solution

Several bisflavins linked at the 10,10'-positions of isoalloxazine rings have been synthesized.The kinetics of the oxidation of N-benzyl-1,4-dihydronicotinamide in aqueous solution have been examined.It has been found that each flavin of a bisflavin is considerably influenced by another intramolecular flavin moiety due to the formation of a charge-transfer complex between intramolecularly reduced and oxidized flavins.The formation of the complex depends on the conformation.

UNUSUAL KINETIC BEHAVIOR OF BIS-FLAVIN FOR N-BENZYL-1,4-DIHYDRONICOTINAMIDE (BNAH) REDUCTION IN AN AQUEOUS SOLUTION

Several bis-flavins linked at 10,10'-positions of isoalloxazine rings were synthesized.The reactivity of each flavin of a bis-flavin was found to be considerably influenced by another intramolecular flavin moiety, depending on the conformation of the bis-