134780-63-5

Upstream product

• 131543-46-9 Glyoxal 
• 87-62-7 2,6-dimethylaniline 
• 24544-04-5 2,6-diisopropylbenzenamine 

Downstream Products

• 107495-79-4 2-Chlor-1,3-bis(2,6-dimethylphenyl)-2-methyl-1,3-diaza-2-sila-4-cyclopenten 
• 107495-83-0 1,4,6,9-Tetrakis(2,6-dimethylphenyl)-1,4,6,9-tetraaza-5-silaspiro<4.4>nonan 
• 84814-10-8 1,3-Bis(2,6-dimethylphenyl)-2,2-dimethyl-1,3-diaza-2-sila-4-cyclopenten 
• 212375-81-0 1,3-bis(2,6-dimethylphenyl)-2-chloro-2,3-dihydro-1H-1,3,2-diazaborole 
• 250285-31-5 1,3-bis-(2,6-dimethylphenyl)-1H-imidazol-3-ium chloride 
• 475578-19-9 1,3-bis(2,6-dimethylphenyl)-4,5-dihydroimidazolinium chloride 
• 90742-41-9 Ru[(CH₃)2C₆H₃NCHCHNC₆H₃(CH₃)2]2Cl₂ 

Relevant academic research and scientific papers

New in situ generated ruthenium catalysts bearing N-heterocyclic carbene ligands for the ring-opening metathesis polymerization of cyclooctene

New 1,3-diarylimidazol(in)ium chlorides bearing phenyl, 1-naphthyl, 4-biphenyl, 2-tolyl, 2,6-dimethylphenyl, and 3,5-dimethylphenyl substituents were synthesized. They were combined with [RuCl2 (p-cymene)] 2 and potassium tert-butoxi

Tuning the Catalyst Reactivity of Imidazolylidene Catalysts through Substituent Effects on the N-Aryl Groups

A series of imidazolium salts with various N-aryl groups were synthesized, and their catalytic activities were evaluated to investigate the contribution of the N-aryl groups to the catalytic activity in the synthesis of γ-butyrolactone through an a3

Tuning the electronic properties of N-heterocyclic carbenes

The electron-donating properties of N-heterocyclic carbenes ([N,N′-bis(2,6-dimethylphenyl)imidazol]-2-ylidene and the respective dihydro ligands) with 4,4′-R-substituted aryl rings (4,4′-R = NEt2, OC12H25, Me, H, Br, S(4-t

1,3-Diarylimidazolidin-2-ylidene (NHC) complexes of Pd(II): Electronic effects on cross-coupling reactions and thermal decompositions

The synthesis of 1,3-diarylimidazolidin-2-ylidene (NHC) precursor, 1,3-bis(2,4,6-trimethylphenyl)imidazolinium chloride, (3b) has been extended to the electronically and sterically modified NHC precursors 3a (X = H), 3c (X = Br) and 3e (X = Cl) in order t

Voltammetric study of interaction of copper with some methyl-substituted ethylenediimine compounds using nonlinear least-squares-Excel-solver

The complex formation of Cu2+ with some recently synthesized methyl-substituted ethylenediimines in binary dimethylformamide-ethanol mixtures was studied by differential pulse voltammetry. The stoichiometry and the stability of the complexes we

Bis(diazadiene)metal(0) Complexes, IV. Nickel(0)-bis(chelates) with Aromatic N-Substituents

With N-aromatic substituted diazadienes (DAD) (R1, R2 = H, CH3 and R3 = R4 = aryl) nickel(0) forms complexes of composition (DAD)2Ni which are prepared preferably by reduction of Ni(II) salts in the pr