1422046-85-2

Basic information

• Product Name: N-(2-hydroxy-3,5-di-tert-butylphenyl)-3-(2-hydroxy-3,5-di-tert-butyl-phenyl)amino-2-nitro-2-propeneimine
• Synonyms: N-(2-hydroxy-3,5-di-tert-butylphenyl)-3-(2-hydroxy-3,5-di-tert-butyl-phenyl)amino-2-nitro-2-propeneimine
• CAS NO: 1422046-85-2
• Molecular Weight: 523.716
• Mol File: 1422046-85-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N-(2-hydroxy-3,5-di-tert-butylphenyl)-3-(2-hydroxy-3,5-di-tert-butyl-phenyl)amino-2-nitro-2-propeneimine(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2-hydroxy-3,5-di-tert-butylphenyl)-3-(2-hydroxy-3,5-di-tert-butyl-phenyl)amino-2-nitro-2-propeneimine(1422046-85-2)
• EPA Substance Registry System: N-(2-hydroxy-3,5-di-tert-butylphenyl)-3-(2-hydroxy-3,5-di-tert-butyl-phenyl)amino-2-nitro-2-propeneimine(1422046-85-2)

Safety Data

• Hazardous Substances Data: 1422046-85-2(Hazardous Substances Data)

Upstream product

• 17758-39-3 1-methyl-5-nitropyrimidin-2(1H)-one 
• 1643-39-6 2-amino-4,6-di-tertbutylphenol 

Relevant articles and documents

Copper complexes of the non-innocent β-diketiminate ligand containing phenol groups

A new type of non-innocent β-diketiminate ligand having redox active phenol groups (LH3, fully protonated form) has been developed, and the structure, physical properties and reactivity of the supported copper(ii) complex [CuII(L3-)]- (L3-, fully deprotonated tri-anionic form) as well as the one-electron and two-electron oxidised complexes, [CuII(L?2-)] and [Cu II(L-)]+, have been examined in detail. The two-electron oxidised form [CuII(L-)]+ exhibited hydrogen atom abstraction ability from 1,4-cyclohexadiene (CHD), whereas the one-electron oxidised form CuII(L?2-)] was found to disproportionate into [CuII(L3-)]- and [CuII(L-)]+ during the course of the reaction with CHD.