Glyoxal bis(2,6-diisopropylanil), N,Nμ-Bis(2,6-diisopropylphenyl)-1,4-diazabutadiene, N,Nμ-Bis(2,6-diisopropylphenyl)ethanediimine

Glyoxal  bis(2,6-diisopropylanil),  N,Nμ-Bis(2,6-diisopropylphenyl)-1,4-diazabutadiene,  N,Nμ-Bis(2,6-diisopropylphenyl)ethanediimine
  • CAS No.:74663-75-5
Other grades of this product :
Glyoxal bis(2,6-diisopropylanil), N,Nμ-Bis(2,6-diisopropylphenyl)-1,4-diazabutadiene, N,Nμ-Bis(2,6-diisopropylphenyl)ethanediimine Basic information
Product Name:Glyoxal bis(2,6-diisopropylanil), N,Nμ-Bis(2,6-diisopropylphenyl)-1,4-diazabutadiene, N,Nμ-Bis(2,6-diisopropylphenyl)ethanediimine
Synonyms:N,N'-1,2-Ethanediylidenebis[2,6-bis(1-methylethyl)phenylamine];N,N'-Bis(2,6-diisopropylphenyl)-1,4-diazabutadiene;N,N'-Bis(2,6-diisopropylphenyl)ethanediimine;N,N'-Bis(2,6-diisopropylphenyl)glyoxaldiimine;1,4-Bis(2,6-diisopropylphenyl)-1,4-diaza-1,3-butadiene;N,N'-(1,2-Ethanediylidene)bis(2,6-diisopropylaniline);N,N'-(1,2-Ethanediylidene)bis[2,6-bis(1-methylethyl)benzenamine];N,N'-(Ethane-1,2-diylidene)bis(2,6-diisopropylaniline)
CAS:74663-75-5
MF:C26H36N2
MW:376.58
EINECS:
Product Categories:
Mol File:74663-75-5.mol
Glyoxal bis(2,6-diisopropylanil), N,Nμ-Bis(2,6-diisopropylphenyl)-1,4-diazabutadiene, N,Nμ-Bis(2,6-diisopropylphenyl)ethanediimine Chemical Properties
Melting point 105-109 °C
Boiling point 492.0±55.0 °C(Predicted)
density 0.95
pka1.85±0.50(Predicted)
Safety Information
WGK Germany 3
MSDS Information
Glyoxal bis(2,6-diisopropylanil), N,Nμ-Bis(2,6-diisopropylphenyl)-1,4-diazabutadiene, N,Nμ-Bis(2,6-diisopropylphenyl)ethanediimine Usage And Synthesis
UsesReactant in preparation of derived ruthenium olefin metathesis catalysts 1 N-cyclic carbene ligand 2 Catalyst in: Palladium-catalyzed aerobic alc. oxidn. supported by a-diimine ligands 3 Regioselective alkylation in presence of ruthenium-bisimine catalytic precursors 4 N-arylation of aromatic amines 5 Preparation of ruthenium nitrosyl alpha-diimine and iminoketone complexes as catalysts for transfer hydrogenation of ketones and atom transfer radical polymerization reactions.
Uses
  • Reactant in preparation of derived ruthenium olefin metathesis catalysts
  • N-cyclic carbene ligand
Catalyst in:
  • Palladium-catalyzed aerobic alc. oxidn. supported by a-diimine ligands
  • Regioselective alkylation in presence of ruthenium-bisimine catalytic precursors
  • N-arylation of aromatic amines
  • Preparation of ruthenium nitrosyl alpha-diimine and iminoketone complexes as catalysts for transfer hydrogenation of ketones and atom transfer radical polymerization reactions
Glyoxal bis(2,6-diisopropylanil), N,Nμ-Bis(2,6-diisopropylphenyl)-1,4-diazabutadiene, N,Nμ-Bis(2,6-diisopropylphenyl)ethanediimine Preparation Products And Raw materials

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