4316-56-7

Basic information

• Product Name: (4-Chlorophenyl)diphenylamine
• Synonyms: (4-Chlorophenyl)-diphenylamine;4-chloro-N,N-di(phenyl)aniline
• CAS NO: 4316-56-7
• Molecular Formula: C₁₈H₁₄ClN
• Molecular Weight: 279.76
• Product Categories: White crystalline powder
• Mol File: 4316-56-7.mol
• Article Data: 22

Chemical Properties

• Melting Point: 103~107°C
• Boiling Point: 404.9 °C at 760 mmHg
• Flash Point: 198.7 °C
• Appearance: /
• Density: 1.203 g/cm³
• Vapor Pressure: 9.14E-07mmHg at 25°C
• Refractive Index: 1.651
• PKA: -3.51±0.30(Predicted)
• CAS DataBase Reference: (4-Chlorophenyl)diphenylamine(CAS DataBase Reference)
• NIST Chemistry Reference: (4-Chlorophenyl)diphenylamine(4316-56-7)
• EPA Substance Registry System: (4-Chlorophenyl)diphenylamine(4316-56-7)

Safety Data

• Hazardous Substances Data: 4316-56-7(Hazardous Substances Data)

Usage

General Description

(4-Chlorophenyl)diphenylamine is a chemical compound with the molecular formula C18H14ClN. It is a diphenylamine derivative that is commonly used as an antioxidant and stabilizer in various industrial processes, including the production of rubber, plastics, and lubricants. It acts by inhibiting the oxidation of these materials, thereby extending their shelf life and improving their performance. Additionally, (4-Chlorophenyl)diphenylamine has been studied for its potential use in the treatment of various diseases, including cancer and neurodegenerative disorders, due to its antioxidant and anti-inflammatory properties. However, further research is needed to fully understand its therapeutic 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

• 122-39-4 diphenylamine 
• 106-39-8 bromochlorobenzene 
• 637-87-6 1-Chloro-4-iodobenzene 
• 106-46-7 para-dichlorobenzene 
• 591-50-4 iodobenzene 
• 106-47-8 4-chloro-aniline 
• 62-53-3 aniline 
• 108-86-1 bromobenzene 
• 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 
• 108720-95-2 4-Chlor-3-amino-triphenylamin 

Downstream Products

• 4432-94-4 N,N-bis(phenyl)-4-biphenylamine 
• 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 

Relevant articles and documents

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

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.

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