64042-50-8

Usage

Chemical structure

A 1,2-ethanediamine backbone with diphenylmethylene groups attached to the nitrogen atoms

Appearance

Unknown, but likely a solid or viscous liquid

Solubility

Unknown, but likely soluble in organic solvents

Melting point

Unknown

Boiling point

Unknown

Density

Unknown

Uses

a. Chelating agent in metal ion analysis
b. Ligand in the preparation of coordination compounds
c. Building block in organic synthesis
d. Production of pharmaceuticals and agrochemicals
e. Manufacturing of dyes and pigments
f. Intermediate in the synthesis of other organic compounds
g. Potential applications in catalysis and materials science

Safety

Unknown, but should be handled with care due to its amine functional groups and potential reactivity with other chemicals

Stability

Unknown, but may be sensitive to heat, light, or moisture

Reactivity

Likely to react with acids, bases, and other nucleophiles due to its amine functional groups

Environmental impact

Unknown, but may pose a risk to aquatic life due to its potential for bioaccumulation and toxicity

Regulatory status

Not listed as a hazardous substance, but may be subject to local or regional regulations depending on its use and disposal methods

Storage

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

Disposal

Should be disposed of according to local or regional regulations for hazardous materials, with proper personal protective equipment and safety measures in place

Synonyms

1,2-Ethanediamine,N1,N2-bis(diphenylmethylene)-, N,N'-Bis(2-phenylmethyl)-1,2-ethanediamine, and other variations based on naming conventions.

Upstream product

• 119-61-9 benzophenone 
• 107-15-3 ethylenediamine 
• 13280-16-5 N-(diphenylmethylene)methylamine 

Downstream Products

• 119-61-9 benzophenone 
• 83027-13-8 N,N'-bis(diphenylmethyl)-1,2-ethanediamine 
• 96317-38-3 N,N'-ethylenebis(diphenylketimine)tetracarbonylchromium⁽⁰⁾ 
• 94554-38-8 Mo(CO)4[(C₆H₅)2CNCH₂CH₂NC(C₆H₅)2] 
• 262592-86-9 Cu((C₆H₅)2CNCH₂CH₂NC(C₆H₅)2)2⁽¹⁺⁾*ClO₄^(1-)=Cu((C₆H₅)2CNCH₂CH₂NC(C₆H₅)2)2ClO₄ 
• 1146114-72-8 [PdCl₂((C₆H₅)2CN(C₂H₄)NC(C₆H₅)2)] 
• 1093215-22-5 ((C₆H₅)2CNCH₂CH₂NC(C₆H₅)2)Fe(CH₂Si(CH₃)3)2 
• 1093215-13-4 ((C₆H₅)2CNCH₂CH₂NC(C₆H₅)2)Fe(CH₂Si(CH₃)3)2(NC₅H₅) 
• 1093215-12-3 ((C₆H₅)2CNCH₂CH₂NC(C₆H₅)2)FeBr₂ 
• 1093215-11-2 ((C₆H₅)2CNCH₂CH₂NC(C₆H₅)2)FeCl₂ 
• 1257252-35-9 N,N'-bis(diphenylmethylene)-1,4-butanediamine 
• 1370700-79-0 1,3-dibenzhydrylimidazolinium chloride 
• 1093215-15-6 ((C₆H₅)2CNCH₂CH₂NC(C₆H₅)2)Fe(CH₂Si(CH₃)3)(OC₄H₈)⁽¹⁺⁾*B(C₆H₅)4^(1-)=(C₃₆H₄₃FeN₂OSi)(B(C₆H₅)4) 
• 1093215-20-3 ((C₆H₅)2CNCH₂CH₂NC(C₆H₅)2)Fe(CH₂Si(CH₃)3)(C₆F₅) 

Relevant academic research and scientific papers

Stereochemical Study of Imines and their N-Borane Adducts by 1H, 11B, 13C and 15N NMR

The synthesis and NMR spectra of the N-borane adducts of two diimines, N-borane-bis(α-phenylethylidene)ethylenediamine and N-borane-bis(α-phenylbenzylidene)ethylenediamine, and four imines, N-borane-α-methylethylidene-2-phenylethylamine, two N-borane-α-ph

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

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.

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

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.

New photoluminescent Cu1N4 chromophores. Stabilisation of copper(1) by unconjugated diimines

Two new photoluminescent homoleptic distorted tetrahedral Cu1N4 chromophores with CuII/I potentials of 0.66-0.81 V vs. SCE are isolated by using two unconjugated diimines (2:1 condensates of R1R2C=O and ethylenediamine; R1 = Ph, R2 = H; R1 = R2 = Ph) as ligands. The Royal Society of Chemistry 2000.