855180-11-9

Basic information

• Product Name: 9-phenyl-9H-carbazol-1-amine
• Synonyms: 9-phenyl-9H-carbazol-1-amine
• CAS NO: 855180-11-9
• Molecular Weight: 258.323
• Mol File: 855180-11-9.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 9-phenyl-9H-carbazol-1-amine(CAS DataBase Reference)
• NIST Chemistry Reference: 9-phenyl-9H-carbazol-1-amine(855180-11-9)
• EPA Substance Registry System: 9-phenyl-9H-carbazol-1-amine(855180-11-9)

Safety Data

• Hazardous Substances Data: 855180-11-9(Hazardous Substances Data)

Upstream product

• 31438-22-9 1-nitro-9H-carbazole 
• 86-74-8 9H-carbazole 
• 615-36-1 2-bromoaniline 
• 855179-34-9 1-nitro-9-phenyl-carbazole 

Downstream Products

• 205-95-8 indolo<3,2,1-jk>carbazole 
• 1454710-71-4 C₃₆H₃₀N₂O₂S₂ 
• 1426925-62-3 C₆₀H₄₄N₄Si₂ 
• 1024598-06-8 11-phenyl-11,12-dihydroindolo[2,3-a]carbazole 

Relevant articles and documents

NOVEL COMPOUND AND ORGANIC ELECTROLUMINESCENCE DEVICE INCLUDING THESAME

The present invention relates to a novel indole-based compound having excellent hole injection and transport capabilities, light-emitting capabilities, and the like, and an organic electroluminescence device which includes the indole-based compound in one or more organic material layers thereof so as to improve characteristics such as light-emitting efficiency, driving voltage, and lifespan.

This is a novel compound and an organic electroluminescence element including

The present invention relates to a novel indole-based compound having excellent hole injection and transport capabilities, light-emitting capabilities, and the like, and an organic electroluminescence device which includes the indole-based compound in one or more organic material layers thereof so as to improve characteristics such as light-emitting efficiency, driving voltage, and lifespan.

Carbazole N-substituent effect upon DTMA: Stabilizing and photochromic modulating

Dithienylmaleimide derivatives 7-27 were synthesized by introducing N-substituted carbazole for photo-stabilizing purpose, and the structures were fully confirmed. The photochromism and photo-stability were recorded via UV-vis spectra. Only ortho compounds 8-17 with N-substituents on carbazole moiety showed escalated photochromic change, while compound 7 and the para counterparts 18-27 showed no appreciable photochromism. Additionally, compounds 8-18 exhibited good photo-stability except 17 under 254 nm irradiation. The unstability of 17 may probably due to overrunning hindrance. These photochromic patterns indicated that hindrance and electronic effect mutually paid a decisive influence on the photochromism and photo-stability, which potentially exploited a new way to construct novel photochromic materials with regulable and conceivable performance.