202832-49-3

Basic information

• Product Name: 1,3-Benzenediamine, N,N'-bis(4-methoxyphenyl)-
• CAS NO: 202832-49-3
• Molecular Formula: C20H20N2O2
• Molecular Weight: 320.391
• Mol File: 202832-49-3.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1,3-Benzenediamine, N,N'-bis(4-methoxyphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-Benzenediamine, N,N'-bis(4-methoxyphenyl)-(202832-49-3)
• EPA Substance Registry System: 1,3-Benzenediamine, N,N'-bis(4-methoxyphenyl)-(202832-49-3)

Safety Data

• Hazardous Substances Data: 202832-49-3(Hazardous Substances Data)

Upstream product

• 127-08-2 potassium acetate 
• 104-94-9 4-methoxy-aniline 
• 71-36-3 butan-1-ol 
• 50-30-6 2,6-dichlorobenzoic acid 
• 51-66-1 4-methoxyacetanilide 
• 626-00-6 1,3-Diiodobenzene 
• 99-65-0 meta-dinitrobenzene 
• 699-19-4 4-methoxyphenylmagnesium chloride 
• 108-36-1 1,3-dibromobenzene 

Downstream Products

• 245442-62-0 N,N'-bis-(3-bromo-phenyl)-N,N'-bis-(4-methoxy-phenyl)-benzene-1,3-diamine 
• 919106-05-1 N-benzyl-N-(3-benzylamino-phenyl)-6-chloro-N'-{3-[(4,6-dichloro-[1,3,5]triazin-2-yl)-(4-methoxy-phenyl)-amino]-phenyl}-N'-(4-methoxy-phenyl)-[1,3,5]triazine-2,4-diamine 
• 213014-92-7 C₃₂H₂₄N₁₀O₁₄ 
• 213014-87-0 C₂₀H₂₂N₄O₂ 
• 245442-65-3 C₇₂H₆₄N₆O₆ 
• 245442-64-2 C₅₈H₄₈Br₂N₄O₄ 
• 245442-63-1 C₄₆H₄₂N₄O₄ 
• 255883-48-8 N,N'-bis{4-(4-methoxyanilino)phenyl}-N,N'-bis(4-methoxyphenyl)-1,3-benzenediamine 
• 255883-40-0 C₅₂H₄₄N₄O₄ 
• 919105-99-0 N,N'-bis-(4,6-dichloro-[1,3,5]triazin-2-yl)-N,N'-bis-(4-methoxy-phenyl)-benzene-1,3-diamine 

Relevant articles and documents

A new method for the selective amination of 1,3- and 1,4-dinitrobenzenes and protected nitroanilines leading to polyfunctional 1,3- and 1,4-disubstituted anilines

The addition of functionalized arylmagnesium reagents to dinitrobenzenes and protected nitroanilines at -20°C in THF furnishes after a reductive workup polyfunctional diarylamines in 47-92% yield.

Palladium-catalyzed synthesis of pure, regiodefined polymeric triarylamines

Triarylamine polymers were prepared by palladium-catalyzed amination of aryl halides, and the electrochemical and magnetic properties of these materials were studied. Through a careful evaluation of the catalytic and polymer chemistry involved in this pro