53847-33-9

Basic information

• Product Name: 4-broMo-N-(diphenylMethylene)aniline
• Synonyms: 4-broMo-N-(diphenylMethylene)aniline
• CAS NO: 53847-33-9
• Molecular Formula: C₁₉H₁₄BrN
• Molecular Weight: 336.22516
• Mol File: 53847-33-9.mol
• Article Data: 13

Chemical Properties

• Boiling Point: 417.4±37.0 °C(Predicted)
• Appearance: /
• Density: 1.24±0.1 g/cm3(Predicted)
• PKA: 2.25±0.50(Predicted)
• CAS DataBase Reference: 4-broMo-N-(diphenylMethylene)aniline(CAS DataBase Reference)
• NIST Chemistry Reference: 4-broMo-N-(diphenylMethylene)aniline(53847-33-9)
• EPA Substance Registry System: 4-broMo-N-(diphenylMethylene)aniline(53847-33-9)

Safety Data

• Hazardous Substances Data: 53847-33-9(Hazardous Substances Data)

Upstream product

• 1013-88-3 Benzophenone imine 
• 589-87-7 1,4-bromoiodobenzene 
• 119-61-9 benzophenone 
• 106-40-1 4-bromo-aniline 
• 936630-41-0 (4-bromophenyl)diphenylmethanamine 
• 936630-42-1 diphenyl-p-trifluoromethylphenylmethylamine 
• 108-86-1 bromobenzene 
• 90-90-4 (4-bromophenyl)(phenyl)methanone 
• 127787-74-0 p-bromophenyltrityl chloride 
• 61623-62-9 1-(p-bromophenyl)-1,1-diphenylcarbinol 
• 120264-99-5 Chlordiphenyl<4-(trifluormethyl)phenyl>methan 
• 106-37-6 1.4-dibromobenzene 
• 26456-05-3 10-methylacridinium perchlorate 
• 2051-90-3 Dichlorodiphenylmethane 

Downstream Products

• 1026043-75-3 N-Benzhydrylidene-N'-(4-trimethylsilanyl-phenyl)-benzene-1,4-diamine 
• 106-40-1 4-bromo-aniline 
• 226713-32-2 N₁-(diphenylmethylene)-N₄-phenylbenzene-1,4-diamine 
• 619319-91-4 1,1-diphenyl-N-(4-(trimethylsilyl)phenyl)methanimine 
• 200395-28-4 N-(diphenylmethylene)-N'-(tert-butoxycarbonyl)-N'-(4-bromophenyl)-p-phenylenediamine 
• 226713-57-1 N-(tert-butoxycarbonyl)-N-(4-bromophenyl)-1,4-phenylenediamine 
• 17889-23-5 4-(trimethylsilyl)aniline 
• 409356-84-9 (4-Amino-phenyl)-(4-methoxy-phenyl)-carbamic acid tert-butyl ester 
• 200395-38-6 (4-Amino-phenyl)-(4-trimethylsilanyl-phenyl)-carbamic acid tert-butyl ester 
• 200395-27-3 [4-(Benzhydrylidene-amino)-phenyl]-(4-methoxy-phenyl)-carbamic acid tert-butyl ester 
• 200395-36-4 [4-(Benzhydrylidene-amino)-phenyl]-(4-trimethylsilanyl-phenyl)-carbamic acid tert-butyl ester 
• 200395-20-6 (4-Bromo-phenyl)-{4-[tert-butoxycarbonyl-(4-methoxy-phenyl)-amino]-phenyl}-carbamic acid tert-butyl ester 
• 206656-24-8 {4-[(4-Amino-phenyl)-tert-butoxycarbonyl-amino]-phenyl}-phenyl-carbamic acid tert-butyl ester 

Relevant articles and documents

Copper-Catalysed Electrophilic Amination of Aryl(alkenyl) Boronic Acids with Nitrogen-Containing Hypervalent Iodine (III) Reagent

A copper-catalysed electrophilic N-imination of aryl(alkenyl) boronic acids with a stable hypervalent iodine(III) reagent containing a transferable (diarylmethylene)amino group is developed. The electrophilic C?N cross-coupling reaction proceeds smoothly at room temperature under oxidant-free and base-free conditions, which is further characterized by the broad functional group compatibility, thereof, extending the N-electrophile scope of electrophilic C?N cross-coupling outside the limitation of N?O and N?Cl reagents. (Figure presented.).

COMPOUND, COATING COMPOSITION COMPRISING SAME, ORGANIC LIGHT-EMITTING DEVICE USING SAME AND METHOD FOR PREPARING SAME

The present specification relates to a compound of Chemical Formula 1, a coating composition including the compound of Chemical Formula 1, an organic light emitting device using the same, and a method for manufacturing the same.

PROCESS FOR THE PREPARATION OF AMINOARYL- AND AMINOHETEROARYL BORONIC ACIDS AND ESTERS

The present invention relates to a process for the preparation of aminoaryl- and aminoheteroaryl boronic acids and esters thereof of formula (I) in high yield. The claimed process uses diarylketal formula (V) to generate an arylbromide of formula (III) in which the amino-group is protected as bisarylmethylidenimino-group, which is then transformed into a formula (I) compound.