4316-56-7

Usage

Uses

Used in Rubber Industry:
(4-Chlorophenyl)diphenylamine is used as an antioxidant and stabilizer for improving the durability and performance of rubber products. It prevents the oxidation process that can lead to degradation, ensuring a longer-lasting and more reliable product.
Used in Plastics Industry:
In the plastics industry, (4-Chlorophenyl)diphenylamine serves as an essential stabilizer, protecting plastics from oxidative degradation. This extends the lifespan of plastic materials and maintains their structural integrity over time.
Used in Lubricants Industry:
(4-Chlorophenyl)diphenylamine is utilized as an antioxidant in lubricants to prevent the oxidation of the base oils, which can cause thickening and loss of lubricating properties. This contributes to the efficient functioning and longevity of machinery and engines.
Used in Pharmaceutical Research:
(4-Chlorophenyl)diphenylamine is studied for its potential therapeutic applications in treating various diseases, such as cancer and neurodegenerative disorders, due to its antioxidant and anti-inflammatory properties. However, further research is necessary to fully explore and understand its potential in these areas.

InChI:InChI=1/C18H14ClN/c19-15-11-13-18(14-12-15)20(16-7-3-1-4-8-16)17-9-5-2-6-10-17/h1-14H

Upstream product

• 62-53-3 aniline 
• 108-86-1 bromobenzene 
• 106-47-8 4-chloro-aniline 
• 108-90-7 chlorobenzene 
• 104-12-1 p-chlorphenylisocyanate 
• 88284-48-4 2-(trimethylsilyl)phenyl trifluoromethanesulfonate 
• 97-00-7 1-chloro-2,4-dinitro-benzene 
• 110155-11-8 4-Chlor-3-nitro-triphenylamin 
• 591-50-4 iodobenzene 
• 106-39-8 bromochlorobenzene 
• 122-39-4 diphenylamine 
• 108720-95-2 4-Chlor-3-amino-triphenylamin 
• 541-73-1 1,3-Dichlorobenzene 
• 106-46-7 para-dichlorobenzene 

Downstream Products

• 267221-88-5 4-(diphenylamino)phenylboronic pinacol ester 
• 19264-71-2 9-(4-chlorophenyl)-9H-carbazole 
• 1221237-14-4 C₆₂H₄₇N₃ 
• 1284216-66-5 1-(4-(diphenylamino)phenyl)ethanone 
• 2350-01-8 4-aminotriphenylamine 
• 19606-98-5 N,N,N'-triphenyl-p-phenylenediamine 
• 4432-94-4 N,N-bis(phenyl)-4-biphenylamine 

Relevant academic research and scientific papers

Arylamine-based organic compound and organic electroluminescent device containing same

The invention relates to the technical field of semiconductor materials, in particular to an arylamine organic compound and an organic electroluminescent device containing the same. The structure of the compound is shown in the general formula (I). The ar

Organic compound, electronic component and electronic device

The invention belongs to the technical field of organic materials, and provides an organic compound, an electronic component and an electronic device. The organic compound has the structure shown in the formula 1, in the formula 1, ring A is a fused aromatic ring with the carbon atom number being 10-14, and ring B is a benzene ring or a fused aromatic ring with the carbon atom number being 10-14; the organic compound of the present invention can improve the performance of an electronic device.

DIARYL AMINE COMPOUND AND METHOD FOR PRODUCING THE SAME

The present invention relates to a process for the preparation of diaryl amine compounds. A compound represented by chemical formula 1, a compound represented by chemical formula 2, and a synthetic reagent in a solvent, the synthetic reagent being CsF, KF, 18 - crown -6, K. 2 CO3, [TBAT] The present invention relates to a process for the preparation of diaryl amine compounds comprising a material selected from the group consisting of a (tetrabutylammonium difluorotriphenylsilicate), TBAF (tetrabutylammonium fluoride) and combinations thereof. Chemical Formula 1. Chemical Formula 2. The diaryl amine compound can be synthesized under the absence of a transition metal to be used to synthesize diaryl amine compounds having various substituents.

Diamine derivative and organic electroluminescent device thereof

The invention provides a diamine derivative and an organic electroluminescent device thereof, and relates to the technical field of organic electroluminescent materials. The diamine derivative represented by Formula 1 contains 9 -fluorene-substituted carbazole functional group, and the hole transport region or cover layer of the organic electroluminescent device of the present invention contains the carbazole derivative of Formula 1. The diamine derivative represented by the formula 1 has better hole transport performance and stability, and the prepared organic electroluminescent device containing the diamine derivative of the formula 1 in the prepared hole transport region exhibits high luminous efficiency. A longer service life and is a lower driving voltage. In addition, the diamine derivative of the formula 1 is also a better cover layer material; the prepared cover layer contains the diamine derivative of the formula 1; the organic electroluminescent device has high luminous efficiency and long service life.

Transition-Metal-Free Diarylation of Isocyanates with Arynes

A facile method for the transition-metal-free diarylation of isocyanates with arynes in the presence of cesium fluoride has been developed, which affords functionalized diaryl amines in moderate to excellent yields. This reaction has good functional group tolerance and provides excellent regioselectivity by utilizing a methoxy-substituted aryne precursor.

COMPOUND FOR ORGANIC ELECTRIC ELEMENT, ORGANIC ELECTRIC ELEMENT COMPRISING THE SAME AND ELECTRONIC DEVICE THEREOF

Disclosed are an organic electronic element comprising: a compound represented by chemical formula 1; a first electrode; a second electrode; and an organic layer located between the first electrode and the second electrode, and an electronic device comprising the organic electronic element. By comprising the compound represented by chemical formula 1 in the organic layer, it is possible to lower a driving voltage, improve luminous efficiency, and expand lifespan of the organic electronic element.COPYRIGHT KIPO 2019

Electron-Catalyzed Coupling of Magnesium Amides with Aryl Iodides

An electron was found to catalyze the coupling of magnesium diarylamides with aryl iodides giving triarylamines through a radical-anion intermediate. The transformation requires no transition metal catalysts or additives, and a wide array of products are formed in good-to-excellent yields.

PdCl2(Ph3P)2/Salicylaldimine Catalyzed Diarylation of Anilines with Unactivated Aryl Chlorides

Triphenylphosphine and salicylaldimine could be used as a mixed ligand system to obtain a high catalytic activity for palladium catalyzed diarylation of primary anilines with unactivated aryl chlorides by the synergistic effect of ligands. The activity and selectivity of the catalytic system could be improved by modifying the structure of salicylaldimine. In refluxing o-xylene, PdCl2(Ph3P)2 with 2,5-ditrifluoromethyl N-phenylsalicylaldimine as a coligand shows high efficiency for the diarylation of various anilines. The catalytic system shows good toleration for the steric hindrance of the substrates. The facile catalytic system works as well on the multiple arylation of 1,1′-biphenyl- 4,4′-diamine with aryl chlorides to afford N,N,N′,N′-tetraaryl-1,1′-biphenyl-4,4′-diamines which are important intermediates of organic light emitting diode (OLED) hole transport materials.

Photochemical Synthesis of Complex Carbazoles: Evaluation of Electronic Effects in Both UV- and Visible-Light Methods in Continuous Flow

An evaluation of both a visible-light- and UV-light-mediated synthesis of carbazoles from various triarylamines with differing electronic properties under continuous-flow conditions has been conducted. In general, triarylamines bearing electron-rich groups tend to produce higher yields than triarylamines possessing electron-withdrawing groups. The incorporation of nitrogen-based heterocycles, as well as halogen-containing arenes in carbazole skeletons, was well tolerated, and often synthetically useful complementarity was observed between the UV-light and visible-light (photoredox) methods.

Method for producing hydroxytriarylamine (by machine translation)

PROBLEM TO BE SOLVED: To economically provide arylamines such as triarylamine. SOLUTION: An arylamine compound represented by formula (1) and an aryl compound having a leaving group represented by formula (2): X-Ar2-X1, are subjected to an arylamination reaction in the presence of a basic group, an alkaline metal salt and/or an alkaline earth metal salt, and an iron catalyst to thereby obtain arylamines such as triarylamines. In formula (1), Ar and Ar1are identical or different, and denote a substituted or non-substituted aryl group, and may be ring-condensed; and a denotes 1 or 2. In formula (2), X and X1are identical or different, and denote at least one leaving group selected from the group consisting of H or Br, I, CMs (mesylate), OTf (triflate) and OTs (tosylate), provided that X and X1are not simultaneously H, and have at least one leaving group; and Ar2denotes a substituted or non-substituted aryl group. COPYRIGHT: (C)2012,JPO&INPIT