78943-59-6

Basic information

• Product Name: N-phenyldibenzazepine
• Synonyms: N-phenyldibenzazepine
• CAS NO: 78943-59-6
• Molecular Weight: 269.346
• Mol File: 78943-59-6.mol
• Article Data: 14

Chemical Properties

• CAS DataBase Reference: N-phenyldibenzazepine(CAS DataBase Reference)
• NIST Chemistry Reference: N-phenyldibenzazepine(78943-59-6)
• EPA Substance Registry System: N-phenyldibenzazepine(78943-59-6)

Safety Data

• Hazardous Substances Data: 78943-59-6(Hazardous Substances Data)

Upstream product

• 10336-24-0 10-phenyl-9,10-dihydroacridine 
• 18107-18-1 diazomethyl-trimethyl-silane 
• 5472-23-1 10-phenylacridin-9(10H)-one 
• 578-95-0 10H-acridin-9-one 
• 108-86-1 bromobenzene 
• 256-96-2 dibenzoazepine 
• 108-90-7 chlorobenzene 
• 108474-32-4 (E/Z)-α,α'-dibromostilbene 
• 62-53-3 aniline 
• 56667-12-0 (Z)-2,2'-dibromostilbene 
• 3433-80-5 1-Bromo-2-bromomethyl-benzene 
• 36901-75-4 (2-bromobenzyl)triphenylphosphonium bromide 
• 591-50-4 iodobenzene 
• 494-19-9 9,10-dihydrodibenzazepine 

Downstream Products

• 1283741-53-6 C₂₆H₁₉NS 
• 1283741-54-7 5-(2-(4-(5H-dibenzo[b,f]azepin-5-yl)phenyl)vinyl)thiophen-2-carbaldehyde 
• 1283741-46-7 3-(5-(4-(5H-dibenzo[b,f]azepin-5-yl)phenyl)thiophen-2-yl)-2-cyanoacrylic acid 
• 1283741-45-6 3-(5-(4-(5H-dibenzo[b,f]azepin-5-yl)styryl)thiophene-2-yl)-2-cyanoacrylic acid 
• 212385-54-1 5-(4-bromophenyl)-5H-dibenzo[b,f]azepine 
• 187731-56-2 4-(5H-dibenzo[b,f]azepin-5-yl)benzaldehyde 

Relevant articles and documents

Dibenzoazepine compound, polymer and application of dibenzoazepine compound and polymer

The invention relates to a dibenzoazepine compound, a polymer and an application of the dibenzoazepine compound and the polymer. The structural formula is shown as a formula (I). The dibenzoazepine compound takes a dibenzoazepine unit as a core and is combined with an outer side unit, so that the dibenzoazepine compound has good hole transport capacity, good film-forming property and thermal stability, and is suitable for preparing an OLED with good photoelectric property.

A general and mild Cu-catalytic: N -arylation of iminodibenzyls and iminostilbenes using unactivated aryl halides

A ligand-free, highly efficient Cu-catalytic N-arylation of iminodibenzyl and iminostilbene derivatives with a broad scope of unactivated aryl halides under mild conditions has been developed for the first time. Moreover, the first Ni-based catalytic syst

Novel method for nickel-catalyzed imino dibenzyl derivative amination

The invention relates to a novel method which can smoothly catalyze an organic light emitting diodes (OLEDs) material unit - imino dibenzyl derivative to undergo amination with iodo- or bromo- arene under mild conditions by using a cheap and easily-obtain