204203-16-7

Basic information

• Product Name: 2,6-Bis[1-[(2,6-diMethylphenyl)iMino]ethyl]pyridine
• Synonyms: 2,6-Bis[1-[(2,6-diMethylphenyl)iMino]ethyl]pyridine;N,N'-(Pyridine-2,6-diylbis(ethan-1-yl-1-ylidene))bis(2,6-dimethylaniline)
• CAS NO: 204203-16-7
• Molecular Formula: C₂₅H₂₇N₃
• Molecular Weight: 369.50198
• Mol File: 204203-16-7.mol
• Article Data: 13

Chemical Properties

• Appearance: /
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 2,6-Bis[1-[(2,6-diMethylphenyl)iMino]ethyl]pyridine(CAS DataBase Reference)
• NIST Chemistry Reference: 2,6-Bis[1-[(2,6-diMethylphenyl)iMino]ethyl]pyridine(204203-16-7)
• EPA Substance Registry System: 2,6-Bis[1-[(2,6-diMethylphenyl)iMino]ethyl]pyridine(204203-16-7)

Safety Data

• Hazardous Substances Data: 204203-16-7(Hazardous Substances Data)

Usage

General Description

2,6-Bis[1-[(2,6-diMethylphenyl)iMino]ethyl]pyridine is a complex chemical compound with the molecular formula C26H30N2. It is commonly used as a ligand in coordination chemistry and catalysis due to its ability to form stable complexes with metal ions. 2,6-Bis[1-[(2,6-diMethylphenyl)iMino]ethyl]pyridine has a pyridine core with two side arms containing imino groups, which serve as binding sites for metal atoms. 2,6-Bis[1-[(2,6-diMethylphenyl)iMino]ethyl]pyridine is known for its versatile coordination behavior, and it has been utilized in various synthetic and catalytic applications in organic chemistry. Its unique structure and reactivity make it an important compound in the field of inorganic and organometallic chemistry.

Upstream product

• 1129-30-2 2,6-Diacetylpyridine 
• 87-62-7 2,6-dimethylaniline 
• 943854-83-9 dichloro(2,6-bis[1-(2,6-dimethylphenylimino)ethyl]pyridine)iron(II) 
• 15658-60-3 diethyl-2,6-pyridinedicarbonyl ester 

Downstream Products

• 1214787-10-6 [^MePDI]FeBr₂ 
• 1214786-98-7 [[(1,1'-(pyridine-2,6-diyl)bis(N-(2,6-dimethylphenyl)ethan-1-imine))Fe(N₂)]₂(μ₂-N₂)] 
• 943854-83-9 dichloro(2,6-bis[1-(2,6-dimethylphenylimino)ethyl]pyridine)iron(II) 
• 455894-32-3 (2,6-bis(1-(2,6-dimethylphenylimino)ethyl)pyridine)Cd(NO₃)2 
• 374072-88-5 [Ir(C₂₅H₂₇N₃)Cl] 
• 474082-43-4 (2,6-bis[1-(2,6-dimethylphenylimino)ethyl]pyridine) Pb(II)(thiocyanate)BF₄ 
• 463931-98-8 [2,6-((2,6-Me₂C₆H₃)N=CMe)₂C₅H₃N]V^IIICl₃ 
• 462661-93-4 (2,6-bis[1-((2,6-dimethylphenyl)imino)ethyl]pyridine)trichlorochromium(III) 
• 226721-85-3 (acetonitrile)dichloro(2,6-bis[1-(2,6-dimethylphenylimino)ethyl]pyridine)ruthenium(II) 
• 1341192-59-3 2-[2,6-(CH₃)2C₆H₃N=C(CH₃)]-6-[2,6-(CH₃)2C₆H₃NHC(CH₃)2](C₅H₃N) 
• 1341192-62-8 C₂₇H₃₅N₃ 
• 501006-80-0 [(2,6-bis[1-(2,6-dimethylphenylimino)ethyl]pyridine)CuCl₂] 
• 844642-16-6 [Co(CH₂Si(CH₃)3)(C₅H₃N(C(CH₃)N(C₆H₃(CH₃)2))2)] 

Relevant articles and documents

Study of an S = 1 NiII pincer electrocatalyst precursor for aqueous hydrogen production based on paramagnetic 1H NMR

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One-Pot, One-Step Precatalysts through Mechanochemistry

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Determination of zero-field splitting in Co2+ halide complexes with magnetic and far-IR measurements

Three penta-coordinate Co2+ complexes with halide substitutes were synthesized. Their zero-field splitting (ZFS) parameters were determined by fitting dc magnetic data and far-infrared magneto-transmission spectra. The results gave an unusual c