204327-05-9

Basic information

• Product Name: [1,1'-Biphenyl]-4-amine, 4'-bromo-N-(3-methylphenyl)-N-phenyl-
• CAS NO: 204327-05-9
• Molecular Formula: C25H20BrN
• Molecular Weight: 414.344
• Mol File: 204327-05-9.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: [1,1'-Biphenyl]-4-amine, 4'-bromo-N-(3-methylphenyl)-N-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: [1,1'-Biphenyl]-4-amine, 4'-bromo-N-(3-methylphenyl)-N-phenyl-(204327-05-9)
• EPA Substance Registry System: [1,1'-Biphenyl]-4-amine, 4'-bromo-N-(3-methylphenyl)-N-phenyl-(204327-05-9)

Safety Data

• Hazardous Substances Data: 204327-05-9(Hazardous Substances Data)

Upstream product

• 1205-64-7 3-Methyldiphenylamine 
• 105946-82-5 4-bromo-4'-iodobiphenyl 
• 92-66-0 4-bromo-1,1'-biphenyl 

Downstream Products

• 872352-26-6 N-(4'-ethynyl-4-biphenyl)-N-(3-tolyl)phenylamine 
• 792909-34-3 2-(4-[4'-(phenyl-m-tolylamino)-4-biphenylyl])-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 433716-27-9 3-[4-(3-methyl{4'-[3-methyl(phenyl)anilino][1,1'-biphenyl]-4-yl}anilino)phenoxy]propyl methacrylate 
• 464216-89-5 3-[4-(3-methyl{4'-[3-methyl(phenyl)anilino][1,1'-biphenyl]-4-yl}anilino)phenoxy]propan-1-ol 
• 195443-34-6 N-(3-methylphenyl)-N-phenyl-4-iodo-1,1'-biphenyl-4'-amine 

Relevant articles and documents

Synthesis of photo-crosslinkable hole-transport polymers with tunable oxidation potentials and their use in organic light-emitting diodes

A series of photo-crosslinkable arylamine-based hole-transport copolymers has been synthesized. The synthetic methodology employed allows for the redox potential of the polymer to be tuned by the incorporation of electron-donating or -withdrawing moieties. Upon exposure to ultraviolet radiation, the polymers become insoluble, as evidenced by UV/Vis absorption spectroscopy, a feature that is useful for the fabrication of multilayer organic light-emitting diodes (OLEDs) by solution processing techniques. OLEDs based on these hole-transport polymers have been fabricated and the performance of the devices has been evaluated. The photo-crosslinking process has been optimized so that it no longer adversely impacts device performance.