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74663-75-5

74663-75-5 Structure

74663-75-5 Structure
IdentificationBack Directory
[Name]

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

74663-75-5
[Synonyms]

(1E,2E)-1,2-Bis(2,6-DiisopropyL
Glyoxal bis[(2,6-diisopropylphenyl)imine]
N,N'-Bis(2,6-diisopropylphenyl)ethanediimine
N,N'-Bis(2,6-diisopropylphenyl)glyoxaldiimine
N,N'-Bis(2,6-diisopropylphenyl)-1,2-ethanediimine
N,N'-Bis(2,6-diisopropylphenyl)ethane-1,2-diimine
(1E,2E)-1,2-Bis(2,6-Diisopropylphenylimino)ethane
N,N'-Bis(2,6-diisopropylphenyl)-1,4-diazabutadiene
(1E,2E)-1,2-Bis(2,6-Diisopropylphenylimino)ethane 90%
N,N'-(1,2-Ethanediylidene)bis(2,6-diisopropylaniline)
N,N'-bis[2,6-di(propan-2-yl)phenyl]ethane-1,2-diimine
N,N'-(Ethane-1,2-diylidene)bis(2,6-diisopropylaniline)
1,4-Bis(2,6-diisopropylphenyl)-1,4-diaza-1,3-butadiene
N,N'-1,2-Ethanediylidenebis[2,6-bis(1-methylethyl)phenylamine]
Benzenamine,N,N'-1,2-ethanediylidenebis[2,6-bis(1-methylethy...
Benzenamine, N,N'-1,2-ethanediylidenebis[2,6-bis(1-methylethyl)-
N,N'-(1,2-Ethanediylidene)bis[2,6-bis(1-methylethyl)benzenamine]
(N,N'E,N,N'E)-N,N'-(ethane-1,2-diylidene)bis(2,6-diisopropylaniline)
(6E)-N-((E)-2-(2,6-diisopropylphenylimino)ethylidene)-2,6-diisopropylbenzenamine
4-(3-METHYLPHENYL)-1-THIOXO-2,4-DIHYDRO[1,2,4]TRIAZOLO[4,3-A]QUINAZOLIN-5(1H)-ONE
Glyoxal bis(2,6-diisopropylanil), N,Nμ-Bis(2,6-diisopropylphenyl)-1,4-diazabutadiene, N,Nμ-Bis(2,6-diisopropylphenyl)ethanediimine
[Molecular Formula]

C26H36N2
[MDL Number]

MFCD03838856
[MOL File]

74663-75-5.mol
[Molecular Weight]

376.58
Chemical PropertiesBack Directory
[Melting point ]

105-109 °C
[Boiling point ]

492.0±55.0 °C(Predicted)
[density ]

0.95
[pka]

1.85±0.50(Predicted)
Safety DataBack Directory
[Symbol(GHS) ]


GHS05,GHS06
[Signal word ]

Danger
[Hazard statements ]

H300-H310-H314-H318-H330
[Precautionary statements ]

P260-P280-P301+P310-P303+P361+P353-P305+P351+P338-P310
[WGK Germany ]

3
Hazard InformationBack Directory
[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
[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.
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