58047-43-1

Basic information

• Product Name: Benzenamine, 4-iodo-N,N-bis(4-methylphenyl)-
• CAS NO: 58047-43-1
• Molecular Formula: C20H18IN
• Molecular Weight: 399.274
• Mol File: 58047-43-1.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Benzenamine, 4-iodo-N,N-bis(4-methylphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenamine, 4-iodo-N,N-bis(4-methylphenyl)-(58047-43-1)
• EPA Substance Registry System: Benzenamine, 4-iodo-N,N-bis(4-methylphenyl)-(58047-43-1)

Safety Data

• Hazardous Substances Data: 58047-43-1(Hazardous Substances Data)

Upstream product

• 20440-95-3 N-phenyl-di-p-tolylamine 

Downstream Products

• 1378024-76-0 N-(4-(10H-phenothiazine-10-yl)phenyl)-4-methyl-N-(p-tolyl)aniline 
• 326877-36-5 1,2-bis[2,4-dimethyl-5-[4-N,N-bis(4-methylphenyl)amino]phenyl-3-thienyl]-3,3,4,4,5,5-hexafluorocyclopentene 
• 596109-87-4 N,N-di(4-tolyl)-4'-(ethynyl)phenylamine 

Relevant articles and documents

Effect of structural modification on the performances of phenothiazine-dye sensitized solar cells

Three novel dyes DX1, DX2 and DX3 containing phenothiazine are designed and synthesized for dye-sensitized solar cells (DSSCs). Photophysical, electrochemical and photovoltaic properties of the three dyes have been systematically investigated. The results

Design and synthesis of efficient electrogenerated chemiluminescent emitters derived from pyrene

The design and synthesis of novel dendrimeric structures derived from a pyrene core with substituted triphenylamine and carbazole periphery demonstrated how molecular engineering allowed the fine tuning of the electrogenerated chemiluminiscence (ECL) properties. These two compound (Py-CBZ and Py-TPA) in comparison with the parent structures (Py and Py-Core) showed better chemical stability and anti-aggregation capability. At the same time, the photophysical (Absλmax, E00FLλmaxΦFL), photochemical (oxygen quenching), electrochemical (redox potentials) and optoelectronic (HOMO-LUMO gap and their energy position) properties were modulated, resulting in obtaining two highly ECL emitting molecular structures (Py-CBZ and Py-TPA). This study showed that functionalization of organic dyes with redox moieties (with the proper linker and position) improved the radical stability and also, modulated the optoelectronic properties with the concomitant enhancement of the ECL performance and their potential use in applications such as organic light-emitting devices.

Polyaromatic amines. Part 4: Synthesis of poly(ethynyl) linked aromatic amines

The title compounds were synthesised and characterised as part of a study into new aromatic amines for charge transporting materials. Each compound was characterised by cyclic voltammetry. A qualitative estimate of the intramolecular charge mobility was deduced from the difference between the first and second oxidation potentials.