15424-38-1

Usage

Uses

Used in Dye and Pigment Production:
N-PHENYL-9-ANTHRAMINE is utilized as a key intermediate in the synthesis of various dyes and pigments, specifically for imparting red and yellow colors to different materials. Its strong absorption and emission in the visible region make it a preferred choice for these applications.
Used in Fluorescent Tracers:
Due to its fluorescent properties, N-PHENYL-9-ANTHRAMINE is employed as a fluorescent tracer in various scientific and industrial applications where tracking and visualizing specific substances or processes is required.
Used in Organic Light-Emitting Diodes (OLEDs) Development:
N-PHENYL-9-ANTHRAMINE is also being researched for its potential use in the development of OLEDs, where its light-emitting characteristics could contribute to the advancement of display and lighting technologies.
Used in Chemical Research:
In the field of chemical research, N-PHENYL-9-ANTHRAMINE serves as a subject of study for understanding the properties and behavior of organic dyes and their potential applications in various industries.

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

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

Downstream Products

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

Relevant academic research and scientific papers

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.

Organic light emitting material and OLED (organic light-emitting diode) prepared from same

The invention discloses an organic light-emitting material and an OLED (organic light-emitting diode) prepared from the same, and relates to the technical field of organic photoelectric materials. The material exhibits good thermal stability by introducing an anthracene-like rigid structure, the OLED is prepared from the material through diffraction, and the material is particularly used as a main body material of the OLED. The OLED has the characteristics of low driving voltage, high brightness, excellent heat resistance, high efficiency and the like, and is better than existing common OLEDs.

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.

A and quinoline derivatives thereof in organic electroluminescent the application in the field of

The invention relates to a compounded quindoline derivative as shown in the formula (1), wherein Ar1 and Ar2 are respectively independently selected from C6-C40 substituted or unsubstituted aromatic groups, or can be connected to form C3-C40 substituted or unsubstituted fused aromatic groups. The invention also relates to an application of the compound in organic electroluminescence devices, especially to an application of the compound used as a luminescence host material of OLED devices.

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.

Bifunctional organic materials for OLEDs based on Tr?ger's base: Subtle structural changes and significant differences in electroluminescence

Three bifunctional organic materials based on Tr?ger's base (TB) scaffold have been designed, synthesized and their functional utility in OLEDs demonstrated through fabrication of devices. The diarylamino-functionalized TBs, i.e., A-TB, PA-TB and P-TB, are all amorphous with considerably high Tgs and permit modulation of electroluminescence with variation of one of the N-aryl rings, e.g., anthryl to 10-phenylanthryl to pyrenyl. Subtle structural modifications are found to manifest in rare pure yellow EL emission from PA-TB.

Novel Burgess reagent mediated C-to-N aryl migration reaction in nitrones

Nitrones undergo useful transformations with Burgess reagent. The reaction ostensibly involves a [3 + 2] annulation across a σ-bond followed by rearrangement involving C-to-N aryl migration. On the basis of available experimental evidence, plausible mechanisms for the rearrangement and the overall conversion have been proposed.

Trineopentylphosphine: A conformationally flexible ligand for the coupling of sterically demanding substrates in the Buchwald-Hartwig amination and suzuki-miyaura reaction

Trineopentylphosphine (TNpP) in combination with palladium provides a highly effective catalyst for the Buchwald-Hartwig coupling of sterically demanding aryl bromides and chlorides with sterically hindered aniline derivatives. Excellent yields are obtain

Synthesis of OLED materials of several triarylamines by palladium catalysts and their light emitting property

Primary aryl amines reacted with aryl halides to give the secondary aryl amines by the catalysis of [Pd(dba)2/P (t-Bu)3] at 80°C in toluene. Secondary aryl amines reacted with 1-bromo-pyrene and 9-bromo-phenanthrene and 2,7-dibromo-9H-fluorene to afford the OLED material of aminopyrene derivatives and aminophenanthrene derivatives and diamino-9H-fluorene type by the catalysis of [Pd(OAc)2/P(t-Bu) 3] at 120°C in o-xylene. The product structures were established by 1H NMR, 13C NMR, 13C(DEPT), HRMS spectra. Physical properties were examined by UV-vis, PL and DSC spectra.