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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

Basic information Safety Supplier Related

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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Safety Information

WGK Germany 
3
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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

Henan Ruiyun Chang Industrial Co., LTD Gold
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18539434999
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cnhnlxw@163.com
Beijing HwrkChemical Technology Co., Ltd
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010-89508211 18501085097
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sales.bj@hwrkchemical.com
Tetranov Biopharm
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13526569071
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sales@leadmedpharm.com
Shanghai Hanhong Scientific Co.,Ltd.
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021-54306202 13764082696
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info@hanhongsci.com
Wuhan Kaymke Chemical Co., Ltd.,
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027-027-87342388 18086026008
Email
sales@kaymke.com
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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(74663-75-5)Related Product Information