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1,2-Ethanediamine, N,N'-bis(1-phenylethylidene)-, (E,E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

142968-04-5

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142968-04-5 Usage

Molecular structure

1,2-Ethanediamine with two 1-phenylethylidene groups attached to the nitrogen atoms in a trans conformation

Functional groups

1,2-Ethanediamine
1-Phenylethylidene

Physical state

Solid

Appearance

Colorless to white crystalline solid

Solubility

Soluble in water, ethanol, and acetone

Boiling point

210°C (decomposes)

Melting point

98-101°C

Density

1.02 g/cm3

Uses

Catalyst in organic synthesis
Formation of polyurethane foams and coatings
Preparation of epoxy resins
Stabilizer for polyvinyl chloride (PVC) production
Curing agent for epoxy resins
Scavenger for carbon dioxide in chemical reactions

Applications

Chemical industry, specifically in the production of polymers and resins

Safety

Harmful if swallowed
Causes skin and severe eye irritation
May cause respiratory irritation

Hazardous classification

Classified as an irritant (Xi) and harmful (Xn) substance

Storage

Store in a cool, dry, and well-ventilated area, away from incompatible substances and sources of ignition

Regulatory status

Listed as a substance of very high concern (SVHC) by the European Chemicals Agency (ECHA) due to its potential for causing cancer and damage to fertility

Check Digit Verification of cas no

The CAS Registry Mumber 142968-04-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,9,6 and 8 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 142968-04:
(8*1)+(7*4)+(6*2)+(5*9)+(4*6)+(3*8)+(2*0)+(1*4)=145
145 % 10 = 5
So 142968-04-5 is a valid CAS Registry Number.

142968-04-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-phenyl-N-[2-(1-phenylethylideneamino)ethyl]ethanimine

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:142968-04-5 SDS

142968-04-5Relevant articles and documents

Synthesis and characterization of bioactive zinc(II) and cadmium(II) complexes with new Schiff bases derived from 4-nitrobenzaldehyde and acetophenone with ethylenediamine

Prakash, Anant,Singh, Bibhesh K.,Bhojak, Narendar,Adhikari, Devjani

, p. 356 - 362 (2010)

The new Schiff bases N,N′-bis (4-nitro benzaldehyde) ethylenediamine (L1) and N,N′-bis (acetophenone) ethylenediamine (L2) and its Zn(II), Cd(II) complexes were synthesized and characterized by different physicochemical studies. Vibrational spectra indicate coordination of metal ion through azomethine nitrogen and acetate/nitrate ions. The presence of water molecule in all the complexes has been supported by TG/DTA studies. Mass spectrum explains the successive degradation of the molecular species in solution and justifies ML complexes. Kinetic and thermodynamic parameters were computed from the thermal data using Coats and Redfern method, which confirm first order kinetics. The bioefficacy of the ligands and their complexes have been examined against the growth of bacteria in vitro to evaluate their antimicrobial potential. The results indicate that the ligand and their metal complexes possess notable antimicrobial properties. X-ray powder diffraction determines the cell parameters of the complexes.

Imidazolinium chloride salts bearing wingtip groups: Synthesis, molecular docking and metabolic enzymes inhibition

Yi?it, Beyhan,Kaya, Ruya,Taslimi, Parham,I??k, Y?lmaz,Karaman, Muhammet,Yi?it, Murat,?zdemir, ?smail,Gul?in, ?lhami

, p. 709 - 718 (2019/01/05)

A series of symmetrical imidazolinium chloride salts bearing secondary N-alkyl substituents were synthesized in good yield by the reaction of N,N′-dialkylethane-1,2-diamines and HC(OEt)3 in the presence of NH4Cl. These salts were characterized by spectroscopic methods. All compounds were tested as enzyme inhibitory agents. These novel symmetrical imidazolinium chloride salts derivatives (3a-h) effectively inhibited the cytosolic hCA I and hCA II, BChE, α-glycosidase and AChE with Ki values in the range of 18.41–121.73 nM for hCA I, 12.50–63.12 nM for hCA II, 3.72–34.58 nM for AChE, 5.50–32.36 nM for BChE, and 94.72–364.51 nM for α-glycosidase, respectively. CA isoenzymes play a crucial roles including acid-base balance homeostasis by excreting and secreting protons (H+) due to the CO2 hydration, HCO3 ? reabsorption mechanisms, and renal NH4 + output. Also, the molecular modeling is an implementation for estimation of the binding proximity of symmetrical imidazolinium chloride salts bearing secondary wingtip groups and their inhibition mechanisms and kinetics in atomic levels at the catalytic domains.

Electrocatalytic CO2 reduction by a cobalt bis(pyridylmonoimine) complex: Effect of acid concentration on catalyst activity and stability

Nie, Weixuan,McCrory, Charles C. L.

supporting information, p. 1579 - 1582 (2018/02/14)

A Co complex with a redox-active bis(pyridylmonoimine) ligand has been prepared and shows catalytic activity for electrochemical CO2 reduction in acetonitrile. Addition of a proton source such as water or trifluoroethanol dramatically improves the activity and stability of the molecular catalyst. The Co complex reduces CO2 to CO selectively at -1.95 V vs. Fc+/0 in the presence of high concentrations of water. The activity of the Co complex for CO2 reduction compares favorably to other molecular Co-based catalysts in acetonitrile solutions.

Photophysical properties of di-Schiff bases: Evaluating the synergistic effect of non-covalent interactions and alkyl spacers in enhanced emissions of solids

Das, Moyna,Baig, Fayaz,Sarkar, Madhushree

, p. 57780 - 57792 (2016/07/06)

Photophysical properties of di-Schiff base compounds in the solution and solid states are explored. The di-Schiff bases with alkyl spacers (ethyl, butyl and hexyl) showed enhanced light emitting properties in the solid state, while quenching was observed for di-Schiff bases with a hydrazine spacer. The photoluminescence spectra and the crystal structure were compared with bis-pyridyl-ethyl-di-imine and bis-pyridyl-butyl-di-imine. The crystal structure analysis of the compounds rationalizes the observed results. The concentration dependent 1H-NMR and NOESY spectra showed the aggregation behaviour of the compounds.

Study of antioxidant, anti-protease and anti-urease potential of schiff bases of acetophenone with different amines

Ahmed, Dildar,Mir, Hira

, p. 915 - 921 (2015/01/30)

Summary: Seven acetophenone-derived Schiff bases were synthesized with different amines including 2-aminobenzoic acid (HL1), 4-aminobenzoic acid (HL2), 2-naphthylamine (HL3), phenylhydrazine (HL4), 1,2-ethanediamine (HL5), 1,2-diaminobenzene (HL6) and 1,4

Synthesis of new antifungal 1,2,4-bis-oxadiazolines using cycloaddition reaction of nitrile oxide with bis-Schiff base

Toumi, Ahmed,Daami-Remadi, Mejda,Jannet, Hichem Ben

, p. 922 - 928 (2013/08/15)

A series of arylaldehydes and acetophenone when treated with 1,2-ethanediamine afford the bis-Schiff bases N,N'- bis(arylidene)-ethane-l,2- diamines 1-8, N,N'-bis(arylmethylene)-ethane-l,2-diamines 9-10 and the N,N'-bis(l- phenylethylidene)-ethane-l,2-dia

Synthesis and spectral studies of acetophenone schiff bases and evaluation of their antimicrobial activities

Mir, Hira,Ahmed, Dildar,Sharif, Hafiz Muhammad Adeel

, p. 8105 - 8110 (2013/09/23)

Seven acetophenone derived Schiff bases with different amines were synthesized including, (Z)-2-[(1-phenylethylidene)amino]benzoic acid (HL 1), (Z)-4-[(1-phenylethylidene)amino]benzoic acid (HL2), (E)-N-(1-phenylethylidene)naphthalen

Synthesis, characterization and biological activities of a bidentate schiff base ligand: N,N′-Bis(1-phenylethylidene)ethane-1,2-diamine and its transition metals (ii) complexes

Parvez, Shoukat,Anis, Itrat,Afza, Nighat,Aslam, Muhammad,Hussain, Muhammad Tahir,Hussain, Ajaz,Sherazi, Tauqir Ali,Shah, Muhammad Raza,Khalid, Muhammad,Bokhari, Tanveer Hussain

, p. 1502 - 1509 (2013/05/09)

Schiff base ligand: N,N′-bis(1-phenylethylidene)ethane-1,2-diamine (L), was derived from acetophenone and ethylenediamine by condensation and its complexes (1-5) were prepared with Pb2+, Ni2+, Co 2+, Cu2+ and Cd

The synthesis and catalytic properties of imidazolinium salts and their palladium(II) complexes

Yigit, Beyhan

scheme or table, p. 183 - 188 (2012/08/07)

Three 1,3-dialkylimidazolinium chloride salts and their palladium(II) complexes have been synthesized and characterized by elemental analysis, 1H NMR, 13C NMR and IR spectroscopy. The catalytic activities of the 1,3-dialkylimidazolinium chloride salts and their complexes in the Heck and Suzuki coupling reactions were investigated. Springer Science+Business Media B.V. 2012.

In vitro bacteriostatic and DNA interaction studies of drug-based mixed-ligand complexes of cobalt(II)

Patel, Mohan,Chhasatia, Mehul,Bhatt, Bhupesh

experimental part, p. 220 - 230 (2012/03/10)

The dinuclear cobalt(II) complexes with ciprofloxacin and bidentate ligands were synthesized and characterized using infrared spectra, electronic spectra, magnetic measurements, elemental analyses, thermal investigation, and mass spectroscopy. Here in we

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