406729-10-0

Basic information

• Product Name: Benzenamine, N,N-diphenyl-4-[(1E)-2-phenylethenyl]-
• CAS NO: 406729-10-0
• Molecular Formula: C26H21N
• Molecular Weight: 347.459
• Mol File: 406729-10-0.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: Benzenamine, N,N-diphenyl-4-[(1E)-2-phenylethenyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenamine, N,N-diphenyl-4-[(1E)-2-phenylethenyl]-(406729-10-0)
• EPA Substance Registry System: Benzenamine, N,N-diphenyl-4-[(1E)-2-phenylethenyl]-(406729-10-0)

Safety Data

• Hazardous Substances Data: 406729-10-0(Hazardous Substances Data)

Upstream product

• 591-50-4 iodobenzene 
• 1520-21-4 4-vinyl benzylamine 
• 100-39-0 benzyl bromide 
• 1080-32-6 O,O-diethyl benzylphosphonate 
• 4181-05-9 4-(diphenylamino)benzaldehyde 
• 589-15-1 1-bromomethyl-4-bromobenzene 
• 38186-51-5 diethyl (4-bromobenzyl)phosphonate 
• 108-86-1 bromobenzene 
• 100-42-5 styrene 
• 36809-26-4 4-N,N-diphenylamino-1-bromobenzene 
• 13041-70-8 (E)-4-bromostilbene 
• 122-39-4 diphenylamine 
• 603-34-9 N,N-diphenylaminobenzene 

Downstream Products

• 89114-74-9 cis-4-(N,N-diphenylamino)stilbene 

Relevant articles and documents

The synthesis and photophysical properties of novel poly(diarylamino) styrenes

A series of novel diamines linked by varying conjugated bridges were characterized using FTIR, NMR and UV-visible spectroscopy, mass spectrometry and elemental analysis. The photoluminescence and thermal properties of the compounds were related to structure and quantum chemical calculations were employed to study the optimized ground state geometry of the compounds. The diarylamines exhibited blue to green fluorescence emission and displayed high thermal stability and high glass transition temperature. As such, the compounds might be very useful as hole-transporting materials in organic light-emitting diodes.

One-pot sequential N and C arylations: An efficient methodology for the synthesis of trans 4-N,N-diaryl aminostilbenes

(Chemical Equation Presented) A double-amination/intermolecular-Heck- reaction sequence is used as a one-pot methodology for sequential C-N and C-C bond formations. 4-Aminostyrene was coupled with aryl bromides and aryl iodides using a [Pd2(dba)3]/proazaphosphatrane catalyst system (dba = dibenzylideneacetone; see scheme) to form irons 4-N,N-diaryl aminostilbene derivatives in high yields, which are comparable to those of previously reported multistep syntheses.

Fluorescence enhancement of trans-4-aminostilbene by N-phenyl substitutions: The "amino conjugation effect"

The synthesis, structure, and photochemical behavior of the trans isomers of 4-(N-phenylamino)-stilbene (1c), 4-(N-methyl-N-phenylamino)stilbene (1d), 4-(N,N-diphenylamino)stilbene (1e), and 4-(N-(2,6-dimethylphenyl)amino)stilbene (1f) are reported and co