900816-53-7

Basic information

• Product Name: 2,6-bis(1-methylethyl)-N-[1-(2-pyridinyl)ethylidene]phenylamine
• Synonyms: 2,6-bis(1-methylethyl)-N-[1-(2-pyridinyl)ethylidene]phenylamine
• CAS NO: 900816-53-7
• Molecular Weight: 280.413
• Mol File: 900816-53-7.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 2,6-bis(1-methylethyl)-N-[1-(2-pyridinyl)ethylidene]phenylamine(CAS DataBase Reference)
• NIST Chemistry Reference: 2,6-bis(1-methylethyl)-N-[1-(2-pyridinyl)ethylidene]phenylamine(900816-53-7)
• EPA Substance Registry System: 2,6-bis(1-methylethyl)-N-[1-(2-pyridinyl)ethylidene]phenylamine(900816-53-7)

Safety Data

• Hazardous Substances Data: 900816-53-7(Hazardous Substances Data)

Upstream product

• 1122-62-9 2-acetylpyridine 
• 24544-04-5 2,6-diisopropylbenzenamine 

Downstream Products

• 219838-89-8 C₅H₄NCMe₂NH(2,6-diisopropylphenyl) 
• 1204519-94-7 2,6-diisopropyl-N-[1-(pyridin-2-yl)ethyl]aniline 

Relevant articles and documents

Silver(I)-pyridinyl Schiff base complexes: Synthesis, structural characterization and reactivity in ring-opening polymerisation of ε-caprolactone

Reactions of AgO2C2F3with 2-pyridinyl Schiff base ligands bore five novel complexes of the type [(AgO2C2F3)2.L2]: where L?=?L1, (E)-N-(1-(pyridin-2-yl)ethylidene)anili

Topological Evolution in Mercury(II) Schiff Base Complexes Tuned through Alkyl Substitution – Synthesis, Solid-State Structures, and Aggregation-Induced Emission Properties

From two series of Schiff base ligands, (E)-N-(pyridine-2-yl)(CMe=NPhR) and (E)-N-(pyridine-2-yl)(CH=NPhR) [R = H, L1a, L1b; 2-CH3, L2a, L2b; 4-CH3, L3a, L3b; 2,6-(CH3)2, L4a, L4b; 2,6-(C2H5/sub

Pyridinylimine-based nickel(II) and palladium(II) complexes: Preparation, structural characterization and use as alkene polymerization catalysts

Preparation of four dimeric nickel(II) complexes and three monomeric palladium(II) complexes bearing didentate pyridinylimine ligands is described. The solid-state structures of these compounds have been determined by single-crystal X-ray diffraction. After activation with methylaluminoxane (MAO) the nickel compounds were used as catalysts in ethylene polymerization producing nearly linear or primarily methyl-branched polymers. The effect of ligand environment was most evident on degree of branching, while catalytic activity and molecular weight of the polymer were more dependent on the general catalyst composition as well as reaction conditions. Activation of the dichloropalladium(II) complexes with MAO yields highly active catalysts for the polymerization of bicyclo[2.2.1]hept-2-ene (norbornene) whereas only low conversions (4.