54480-44-3

Basic information

• Product Name: 1,4-Benzenediamine, N'-(4-methoxyphenyl)-N,N-dimethyl-
• CAS NO: 54480-44-3
• Molecular Formula: C15H18N2O
• Molecular Weight: 242.321
• Mol File: 54480-44-3.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: 1,4-Benzenediamine, N'-(4-methoxyphenyl)-N,N-dimethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,4-Benzenediamine, N'-(4-methoxyphenyl)-N,N-dimethyl-(54480-44-3)
• EPA Substance Registry System: 1,4-Benzenediamine, N'-(4-methoxyphenyl)-N,N-dimethyl-(54480-44-3)

Safety Data

• Hazardous Substances Data: 54480-44-3(Hazardous Substances Data)

Upstream product

• 101-64-4 Variamin Blau 
• 13139-86-1 4-methoxyphenyl magnesium bromide 
• 138-89-6 p-dimethylaminonitrosobenzene 
• 586-77-6 4-bromo-N,N-dimethylaniline 
• 104-94-9 4-methoxy-aniline 
• 696-62-8 para-iodoanisole 
• 7463-28-7 N'-acetyl-N,N-dimethyl-1,4-phenylenediamine 

Downstream Products

• 350-46-9 4-Fluoronitrobenzene 

Relevant articles and documents

High performance black-to-transmissive electrochromic device with panchromatic absorption based on TiO2-supported viologen and triphenylamine derivatives

A novel black-to-transmissive electrochromic device based on TiO2-supported viologen and triphenylamine derivatives was designed and constructed via the absorption-complementary approach. In the device, cathodically coloring electrochromic mate

An electrochromic material and its preparation method and black electrochromic material and its preparation method

The invention provides an electrochromic material, a preparation method thereof, a black electrochromic material and a preparation method thereof. The electrochromic material has the structure in the formula (I), serves as an electrochromic material of a

Simple, efficient catalyst system for the palladium-catalyzed amination of aryl chlorides, bromides, and triflates

Palladium complexes supported by (o-biphenyl)P(t-Bu)2 (3) or (o- biphenyl)PCy2 (4) are efficient catalysts for the catalytic amination of a wide variety of aryl halides and triflates. Use of ligand 3 allows for the room-temperature catalytic amination of many aryl chloride, bromide, and triflate substrates, while ligand 4 is effective for the amination of functionalized substrates or reactions of acyclic secondary amines. The catalysts perform well for a large number of different substrate combinations at 80-110 °C, including chloropyridines and functionalized aryl halides and triflates using 0.5-1.0 mol % Pd; some reactions proceed efficiently at low catalyst levels (0.05 mol % Pd). These ligands are effective for almost all substrate combinations that have been previously reported with various other ligands, and they represent the most generally effective catalyst system reported to date. Ligands 3 and 4 are air-stable, crystalline solids that are commercially available. Their effectiveness is believed to be due to a combination of steric and electronic properties that promote oxidative addition, Pd-N bond formation, and reductive elimination.