(1E,2E)-1,2-Bis(2,6-Diisopropylphenylimino)ethane

• Catalog No.: 693979
• CAS Number: 74663-75-5
• M. F.: C26H36N2
• M. W.: 376.57744
• Purity: 90%

SYNONYMS

• Title: (1E,2E)-1,2-双(2,6-二异丙苯基亚氨基)乙烷
• IUPAC name: N-(2-{[2,6-bis(propan-2-yl)phenyl]imino}ethylidene)-2,6-bis(propan-2-yl)aniline
• IUPAC Traditional name: N-{2-[(2,6-diisopropylphenyl)imino]ethylidene}-2,6-diisopropylaniline
• Synonyms: Glyoxal bis(2,6-diisopropylanil); 乙二醛双(2,6-二异丙基苯胺); N,N′-双(2,6-二异丙基苯基))-1,4-二氮杂丁二烯; N,N′-Bis(2,6-diisopropylphenyl)-1,4-diazabutadiene; N,N′-Bis(2,6-diisopropylphenyl)ethanediimine; N,N′-双(2,6-二异丙基苯基)乙二亚胺

DATABASE IDS

• MDL Number: MFCD03838856
• CAS Number: 74663-75-5

PROPERTIES

• Linear Formula: (C3H7)2C6H3NCHCHNC6H3(C3H7)2
• Purity: 90%
• Melting Point: 105-109 °C
• German water hazard class: 3

DETAILS

Description (English)

Packaging
1, 5 g in glass bottle
Application

• Reactant in preparation of derived ruthenium olefin metathesis catalysts1
• N-cyclic carbene ligand2Catalyst in:
• Palladium-catalyzed aerobic alc. oxidn. supported by a-diimine ligands3
• Regioselective alkylation in presence of ruthenium-bisimine catalytic precursors4
• N-arylation of aromatic amines5
• Preparation of ruthenium nitrosyl alpha-diimine and iminoketone complexes as catalysts for transfer hydrogenation of ketones and atom transfer radical polymerization reactions6

Description (简体中文)

包装
1, 5 g in glass bottle
Application

• Reactant in preparation of derived ruthenium olefin metathesis catalysts1
• N-cyclic carbene ligand2Catalyst in:
• Palladium-catalyzed aerobic alc. oxidn. supported by a-diimine ligands3
• Regioselective alkylation in presence of ruthenium-bisimine catalytic precursors4
• N-arylation of aromatic amines5
• Preparation of ruthenium nitrosyl alpha-diimine and iminoketone complexes as catalysts for transfer hydrogenation of ketones and atom transfer radical polymerization reactions6