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 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
- Mol File:
- 74663-75-5.mol
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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
- pka
- 1.85±0.50(Predicted)
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Glyoxal bis(2,6-diisopropylanil), N,Nμ-Bis(2,6-diisopropylphenyl)-1,4-diazabutadiene, N,Nμ-Bis(2,6-diisopropylphenyl)ethanediimine Usage And Synthesis
Uses
Reactant 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)ethanediimineSupplier
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