15424-38-1

Basic information

• Product Name: N-PHENYL-9-ANTHRAMINE
• Synonyms: 9-ANILINOANTHRACENE;N-PHENYL-9-ANTHRAMINE;N-(9-Anthracenyl)aniline;N-(Anthracen-9-yl)-N-phenylamine;N-Phenylanthracen-9-amine
• CAS NO: 15424-38-1
• Molecular Formula: C₂₀H₁₅N
• Molecular Weight: 269.34
• Product Categories: Anthracenes
• Mol File: 15424-38-1.mol
• Article Data: 9

Chemical Properties

• Melting Point: 207 °C
• Boiling Point: 434.355 °C at 760 mmHg
• Flash Point: 233.262 °C
• Appearance: /
• Density: 1.204 g/cm³
• Refractive Index: 1.752
• Solubility: almost transparency in Acetone
• PKA: 0.78±0.30(Predicted)
• CAS DataBase Reference: N-PHENYL-9-ANTHRAMINE(CAS DataBase Reference)
• NIST Chemistry Reference: N-PHENYL-9-ANTHRAMINE(15424-38-1)
• EPA Substance Registry System: N-PHENYL-9-ANTHRAMINE(15424-38-1)

Safety Data

• Hazardous Substances Data: 15424-38-1(Hazardous Substances Data)

Usage

General Description

N-PHENYL-9-ANTHRAMINE is a chemical compound with the molecular formula C20H13N. It is an organic dye intermediate that is commonly used in the production of dyes, pigments, and fluorescent tracer compounds. It is a dark red to brown powder that is insoluble in water but soluble in organic solvents. N-PHENYL-9-ANTHRAMINE is known for its strong absorption and emission in the visible region of the electromagnetic spectrum, and it is often used in the production of red and yellow dyes. Additionally, it has been researched for its potential use in the development of organic light-emitting diodes (OLEDs). However, it is important to handle N-PHENYL-9-ANTHRAMINE with care, as it is considered toxic and may cause skin and eye irritation upon contact.

InChI:InChI=1/C20H15N/c1-2-10-17(11-3-1)21-20-18-12-6-4-8-15(18)14-16-9-5-7-13-19(16)20/h1-14,21H

Upstream product

• 716-53-0 9-chloroanthracene 
• 62-53-3 aniline 
• 108-86-1 bromobenzene 
• 779-03-3 9-aminoanthracene 
• 1564-64-3 9-Bromoanthracene 
• 103-84-4 Acetanilid 

Downstream Products

• 105791-33-1 9,9-bis-benzoyloxy-10-phenylimino-9,10-dihydro-anthracene 
• 1255517-95-3 N-(anthracen-9-yl)-6-butyl-N-phenyl-6H-indolo[2,3-b]quinoxalin-9-amine 
• 96766-00-6 N,N'-bis-(4-nitro-phenyl)-[9,9']bianthryl-10,10'-diyldiamine 
• 96378-62-0 10,10-bis-benzoyloxy-anthrone 
• 948309-27-1 5-(7-(anthracen-9-yl(phenyl)amino)-9,9-diethyl-9H-fluoren-2-yl)thiophene-2-carbaldehyde 
• 105820-80-2 9H,9'H-[9,9']bianthryl-10,10'-dione-bis-(4-nitro-phenylimine) 
• 105862-44-0 9H,9'H-[9,9']bianthryl-10,10'-dione-bis-phenylimine 

Relevant articles and documents

Compound, organic light-emitting device, and electronic device

The invention belongs to the technical field of organic materials, and provides a compound with a structure as shown in a chemical formula 1 which is described in the specification. In the chemical formula 1, Ar1, Ar2, Ar3 and Ar4 are H or a group as shown in a chemical formula 1-1, and at least one of Ar1, Ar2, Ar3 and Ar4 is the group as shown in the chemical formula 1-1. As the molecular structure of the compound contains a triarylamine group, and contains an electron-donating triphenylamine part and a molecular large conjugated system, the molecule of the compound has the property of intramolecular charge transfer. An organic light-emitting device prepared from the compound has high device efficiency. Compared with the prior art, an organic electroluminescent material disclosed by theinvention has higher stability, so the service life of an organic electroluminescent device is prolonged. In addition, a phenanthrene fused ring derivative is used for structural modification of an electron donor and an electron acceptor respectively, so the photophysical and electrochemical properties of the material can be effectively regulated and controlled, and a luminescent layer material with a narrow energy level band gap is obtained. The invention further provides the organic light-emitting device and an electronic device.

Aromatic amine derivative, and preparation method and application thereof

The invention provides an aromatic amine derivative, and a preparation method and the application of the aromatic amine derivative, and relates to the technical field of organic optoelectronic materials. Through the design of molecular structure optimization, the aromatic amine derivative provided by the invention has an excellent hole transmitting capacity and can be used for preparing an organic light-emitting device, and particularly by serving as the hole transmitting material of the organic light-emitting device, the aromatic amine derivative shows advantages of high efficiency and long service life, which are superior than those of a conventionally used OLED (Organic Light Emitting Diode) device. The invention further provides a preparation method of the aromatic amine derivative, and the preparation method is simple and raw materials are easy to access.

Phenothiazine class derivative and preparation method and application thereof

The invention provides a phenothiazine class derivative and a preparation method and application thereof and relates to the technical field of organic optoelectronic materials. The optimization of molecular structure design, the phenothiazine class derivative has a better rigid structure and big-pi bond conjugate system and quite good hole-transmission capability and can be used for preparing an organic light-emitting device, and the phenothiazine class derivative high in efficiency and long in service life and serving as hole-transmission material in the organic light-emitting device is prior to an existing OLED (organic light-emitting diode) in common use. The invention further provides the preparation method of the phenothiazine class derivative, and the preparation method is simple, and raw materials are easy to obtain.