36629-08-0

Basic information

• Product Name: 1,4-Benzenediamine, N-(4-nitrophenyl)-N'-phenyl-
• Synonyms: N-(4-nitrophenyl)-N'-phenyl-1,4-phenylenediamine;N-(4-nitrophenyl)-N'-phenyl-benzene-1,4-diamine;N-(4-nitro-phenyl)-N'-phenyl-p-phenylenediamine;1,4-Benzenediamine,N-(4-nitrophenyl)-N'-phenyl;N-(4-Nitro-phenyl)-N'-phenyl-p-phenylendiamin
• CAS NO: 36629-08-0
• Molecular Formula: C18H15N3O2
• Molecular Weight: 305.336
• Mol File: 36629-08-0.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1,4-Benzenediamine, N-(4-nitrophenyl)-N'-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,4-Benzenediamine, N-(4-nitrophenyl)-N'-phenyl-(36629-08-0)
• EPA Substance Registry System: 1,4-Benzenediamine, N-(4-nitrophenyl)-N'-phenyl-(36629-08-0)

Safety Data

• Hazardous Substances Data: 36629-08-0(Hazardous Substances Data)

Upstream product

• 350-46-9 4-Fluoronitrobenzene 
• 101-54-2 N-phenylphenylene-1,4-diamine 

Downstream Products

• 737827-50-8 C₂₄H₂₀N₄O₂ 
• 80471-61-0 N₁-(4-aminophenyl)-N₄-(4-(phenylamino)phenyl)benzene-1,4-diamine 
• 36629-09-1 N¹-(4-aminophenyl)-N₄-phenylbenzene-1,4-diamine 

Relevant articles and documents

On the formation of mauvein: Mechanistic considerations and preparative results

The reaction of aniline (AH2) with an oxidizing agent in acidic solution gives rise to the formation of a mixture of products containing, besides a variety of oligoanilines named as Aniline Black or Polyaniline, Mauvein as a deeply purple phena

Synthesis and spectroscopic properties of aniline tetramers. Comparative studies

A new synthetic method involving SNAr coupling of 4-fluoronitrobenzene to arylamines, followed by the reduction of the nitro groups, has been developed. Two types of aniline oligomers, namely Ph/NH 2 and NH2/NH2