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

• 5467-74-3 4-Bromophenylboronic acid 
• 2051-90-3 Dichlorodiphenylmethane 
• 106-40-1 4-bromo-aniline 
• 26456-05-3 10-methylacridinium perchlorate 
• 1013-88-3 Benzophenone imine 
• 106-37-6 1.4-dibromobenzene 
• 120264-99-5 Chlordiphenyl<4-(trifluormethyl)phenyl>methan 
• 61623-62-9 1-(p-bromophenyl)-1,1-diphenylcarbinol 
• 90-90-4 (4-bromophenyl)(phenyl)methanone 
• 108-86-1 bromobenzene 
• 936630-42-1 diphenyl-p-trifluoromethylphenylmethylamine 
• 936630-41-0 (4-bromophenyl)diphenylmethanamine 
• 119-61-9 benzophenone 
• 589-87-7 1,4-bromoiodobenzene 

Downstream Products

• 1026043-75-3 N-Benzhydrylidene-N'-(4-trimethylsilanyl-phenyl)-benzene-1,4-diamine 
• 106-40-1 4-bromo-aniline 
• 214360-73-3 4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)aniline 
• 206656-23-7 N-(diphenylmethylene)-N'-(tert-butoxycarbonyl)-N'-[4-(N-tert-butoxycarbonylanilino)phenyl]-p-phenylenediamine 
• 206656-24-8 {4-[(4-Amino-phenyl)-tert-butoxycarbonyl-amino]-phenyl}-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 
• 200395-36-4 [4-(Benzhydrylidene-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 
• 200395-38-6 (4-Amino-phenyl)-(4-trimethylsilanyl-phenyl)-carbamic acid tert-butyl ester 
• 409356-84-9 (4-Amino-phenyl)-(4-methoxy-phenyl)-carbamic acid tert-butyl ester 
• 17889-23-5 4-(trimethylsilyl)aniline 
• 226713-57-1 N-(tert-butoxycarbonyl)-N-(4-bromophenyl)-1,4-phenylenediamine 
• 200395-28-4 N-(diphenylmethylene)-N'-(tert-butoxycarbonyl)-N'-(4-bromophenyl)-p-phenylenediamine 

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 of formula (I) in high yields The claimed process uses diarylketal formula (V) to generate an arylbromid of formula (III) in which the amino-group is protected as bisarylmethylidenimino-group: