Basic information Safety Supplier Related

4-BROMO-4'-(DIPHENYLAMINO)BIPHENYL

Basic information Safety Supplier Related

4-BROMO-4'-(DIPHENYLAMINO)BIPHENYL Basic information

Product Name:
4-BROMO-4'-(DIPHENYLAMINO)BIPHENYL
Synonyms:
  • 4'-Bromo-N,N-diphenyl-4-biphenylamine
  • 4-BROMO-4''-(DIPHENYLAMINO)BIPHENYL, 93%(GC)
  • (4'-BROMOBIPHENYL-4-YL)DIPHENYLAMINE
  • N,N-Diphenyl-4'-bromo-1,1'-biphenyl-4-amine
  • 4'-broMo-N,N-diphenylbiphenyl-4-aMine
  • 4-(4-bromophenyl)-N,N-diphenylaniline
  • K0063
  • 4-Bromo-4'-(diphenylamino)biphenyl >
CAS:
202831-65-0
MF:
C24H18BrN
MW:
400.31
EINECS:
1312995-182-4
Product Categories:
  • Acid Anhydrides, etc. (Reagents for Conducting Polymer Research)
  • Functional Materials
  • Reagents for Conducting Polymer Research
Mol File:
202831-65-0.mol
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4-BROMO-4'-(DIPHENYLAMINO)BIPHENYL Chemical Properties

Melting point:
127.0 to 131.0 °C
Boiling point:
518.2±33.0 °C(Predicted)
Density 
1.325
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
form 
powder to crystal
pka
-3.34±0.60(Predicted)
color 
White to Orange to Green
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Safety Information

HS Code 
29214990
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4-BROMO-4'-(DIPHENYLAMINO)BIPHENYL Usage And Synthesis

Synthesis

589-87-7

201802-67-7

202831-65-0

Example 1.13.1 Synthesis of 4'-bromo-N,N-diphenyl-[1,1'-biphenyl]-4-amine (35): (4-(diphenylamino)phenyl)boronic acid (1.5 g, 5.19 mmol), 4-iodo-1-bromobenzene (1.33 g, 4.71 mmol), Na2CO3 (1.78 g, 16.8 mmol) and Pd(PPh3 )4 (0.163 g, 0.141 mmol) were dissolved in THF/H2O (28 mL/17 mL) mixed solvent. The reaction mixture was degassed and heated to reflux under argon protection overnight. After completion of the reaction, it was cooled to room temperature and the mixture was poured into dichloromethane (150 mL) and washed sequentially with water (2 x 150 mL) and brine (100 mL). The organic phase was dried with Na2SO4, filtered and purified by fast column chromatography (silica gel, hexane/ethyl acetate 50:1), and finally recrystallized in a solvent mixture of dichloromethane/methanol to give a white solid product (compound 35) (1.64 g, 87% yield).

References

[1] Journal of Organic Chemistry, 2017, vol. 82, # 18, p. 9435 - 9451
[2] Patent: US2010/326526, 2010, A1
[3] Patent: WO2011/8560, 2011, A1. Location in patent: Page/Page column 47-48
[4] RSC Advances, 2015, vol. 5, # 41, p. 32298 - 32306
[5] Patent: US9172051, 2015, B2. Location in patent: Page/Page column 67; 68; 69; 70; 71; 72; 75; 76

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