144342-87-0

Basic information

• Product Name: Tetraethyl 2,2',2,2'-<<4,4'-bis(4-methoxyphenyl)-2,2'-bipyridine-6,6'-diyl>bis(methylenenitrilo)>tetrakis(acetate)
• CAS NO: 144342-87-0
• Molecular Weight: 770.88
• Mol File: 144342-87-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Tetraethyl 2,2',2,2'-<<4,4'-bis(4-methoxyphenyl)-2,2'-bipyridine-6,6'-diyl>bis(methylenenitrilo)>tetrakis(acetate)(CAS DataBase Reference)
• NIST Chemistry Reference: Tetraethyl 2,2',2,2'-<<4,4'-bis(4-methoxyphenyl)-2,2'-bipyridine-6,6'-diyl>bis(methylenenitrilo)>tetrakis(acetate)(144342-87-0)
• EPA Substance Registry System: Tetraethyl 2,2',2,2'-<<4,4'-bis(4-methoxyphenyl)-2,2'-bipyridine-6,6'-diyl>bis(methylenenitrilo)>tetrakis(acetate)(144342-87-0)

Safety Data

• Hazardous Substances Data: 144342-87-0(Hazardous Substances Data)

Upstream product

• 117330-45-7 4,4'-Bis(4-methoxyphenyl)-2,2'-bipyridine-6,6'-dimethyl diacetate 
• 117330-44-6 4,4'-Bis(4-methoxyphenyl)-6,6'-dimethyl-2,2'-bipyridine N,N'-dioxide 
• 144342-67-6 4,4'-Bis(4-methoxyphenyl)-2,2'-bipyridine-6,6'-dimethanol 
• 116772-94-2 4,4'-Bis(4-methoxyphenyl)-6,6'-dimethyl-2,2'-bipyridine 
• 6290-05-7 Diethyl iminodiacetate 
• 144342-71-2 6,6'-Bis(chloromethyl)-4,4'-bis(4-methoxyphenyl)-2,2'-bipyridine 

Downstream Products

• 144343-03-3 2,2',2,2'-<<4,4'-Bis(4-methoxyphenyl)-2,2'-bipyridine-6,6'-diyl>bis(methylenenitrilo)>tetrakis(acetic acid) 

Relevant articles and documents

New 2,2'-Bipyridine Derivatives and Their Luminescence Properties with Europium(III) and Terbium(III) Ions

Twenty differently substituted 2,2',2",2"'-III and TbIII ions.The relative luminescence yields, excitation maxima, and emission decay constants were determined for the corresponding EuIII and TbIII chelates.The substituents at the bipyridine moiety had a significant effect on the luminescence properties: the best relative luminescence yields R were obtained for ligands with electron-donating substituents (e.g.Me, Ph), electron-withdrawing substituents (e.g.NO2, COOH) had a reverse effect.However, no clear correlation between the relative luminescence yields and the substituent parameters was found.