4,4'-DIBROMOTRIPHENYLAMINE

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Products Intro: Product Name:4,4'-Dibromotriphenylamine
CAS:81090-53-1
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Products Intro: Product Name:4-Bromo-N-(4-bromophenyl)-N-phenylaniline
CAS:81090-53-1
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Products Intro: Product Name:4,4'-DIBROMOTRIPHENYLAMINE
CAS:81090-53-1
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Products Intro: CAS:81090-53-1
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4,4'-DIBROMOTRIPHENYLAMINE manufacturers

4,4'-DIBROMOTRIPHENYLAMINE Basic information
Product Name:4,4'-DIBROMOTRIPHENYLAMINE
Synonyms:N,N-BIS(P-BROMOPHENYL)ANILINE;Dibromotriphenylamine;4,4''-DIBROMOTRIPHENYLAMINE 98+%;N,N-Bis(4-bromophenyl)aniline;4,4'-(Phenylimino)bis(1-bromobenzene);Bis(4-bromophenyl)phenylamine;Phenylbis(4-bromophenyl)amine;N,N-Diphenyl-4,4'-dibromoaniline
CAS:81090-53-1
MF:C18H13Br2N
MW:403.11
EINECS:628-703-3
Product Categories:OLED materials,pharm chemical,electronic;Acid Anhydrides, etc. (Reagents for Conducting Polymer Research);Electroluminescence;Fluorenes, etc. (reagent for high-performance polymer research);Functional Materials;Reagent for High-Performance Polymer Research;Reagents for Conducting Polymer Research
Mol File:81090-53-1.mol
4,4'-DIBROMOTRIPHENYLAMINE Structure
4,4'-DIBROMOTRIPHENYLAMINE Chemical Properties
Melting point 69°C
Boiling point 470.7±30.0 °C(Predicted)
density 1.593
Fp 110 °C
storage temp. Inert atmosphere,Room Temperature
pka-4.29±0.50(Predicted)
form Solid
color Off-white
InChIInChI=1S/C18H13Br2N/c19-14-6-10-17(11-7-14)21(16-4-2-1-3-5-16)18-12-8-15(20)9-13-18/h1-13H
InChIKeyKIGVOJUDEQXKII-UHFFFAOYSA-N
SMILESC1(N(C2=CC=C(Br)C=C2)C2=CC=CC=C2)=CC=C(Br)C=C1
Safety Information
Hazard Codes Xn
Risk Statements 36/37/38-43-22
Safety Statements 26-36/37/39-36/37
WGK Germany 3
HS Code 29214990
MSDS Information
4,4'-DIBROMOTRIPHENYLAMINE Usage And Synthesis
UsesPolytriarylamine Semiconductors
Synthesis
Triphenylamine

603-34-9

4,4'-DIBROMOTRIPHENYLAMINE

81090-53-1

Step 1: Synthesis of 4,4'-dibromotriphenylamine 1. 12 g (50 mmol) of triphenylamine was dissolved in 250 mL of ethyl acetate in a 500 mL conical flask. 2. 18 g (100 mmol) of N-bromosuccinimide (NBS) was added to the above solution. 3. The reaction mixture was stirred at room temperature for 24 hours. 4. Upon completion of the reaction, the reaction mixture was washed with deionized water. 5. The mixture was dried by adding anhydrous magnesium sulfate to remove water. 6. The desiccant was removed by filtration and the filtrate was concentrated. 7. 7. 20 g of white solid product was obtained after drying in 99% yield.

References[1] Patent: WO2009/72587, 2009, A1. Location in patent: Page/Page column 191
[2] Patent: WO2009/139358, 2009, A1. Location in patent: Page/Page column 90
[3] Journal of Materials Chemistry C, 2016, vol. 4, # 13, p. 2579 - 2586
[4] Journal of Materials Chemistry C, 2016, vol. 4, # 43, p. 10301 - 10308
[5] Journal of Materials Chemistry, 2012, vol. 22, # 23, p. 11629 - 11635
4,4'-DIBROMOTRIPHENYLAMINE Preparation Products And Raw materials
Raw materialsTriphenylamine-->Ethyl acetate-->N-Bromosuccinimide
Tag:4,4'-DIBROMOTRIPHENYLAMINE(81090-53-1) Related Product Information
Propantheline bromide C60MC12 Triphenylamine 4,4'-DIBROMOTRIPHENYLAMINE TRIS(4-BROMOPHENYL)AMINIUM HEXACHLOROANTIMONATE 4,4'-DIBROMO-4''-PHENYLTRIPHENYLAMINE 4,4'-DIBROMO-4''-CYCLOHEXYLTRIPHENYLAMINE Tris(4-bromophenyl)amine

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