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3-broMo-6,9-diphenyl-9H-carbazole

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3-broMo-6,9-diphenyl-9H-carbazole Basic information

Product Name:
3-broMo-6,9-diphenyl-9H-carbazole
Synonyms:
  • 3-broMo-6,9-diphenyl-9H-carbazole
  • 3-Bromo-6,9-diphenylcarbazole
  • DPCBA-B
  • 3-Bromo-6,9-diphenylcarbazole>
  • 9H-Carbazole, 3-bromo-6,9-diphenyl-
  • 3-broMo-6,9-diphenyl-9H-carbazole ISO 9001:2015 REACH
CAS:
1160294-85-8
MF:
C24H16BrN
MW:
398.29
Mol File:
1160294-85-8.mol
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3-broMo-6,9-diphenyl-9H-carbazole Chemical Properties

Melting point:
143.0 to 147.0 °C
Boiling point:
564.2±32.0 °C(Predicted)
Density 
1.32±0.1 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
solubility 
soluble in Toluene
form 
powder to crystal
color 
White to Almost white
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Safety Information

HS Code 
2933.99.8290
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3-broMo-6,9-diphenyl-9H-carbazole Usage And Synthesis

Chemical Properties

white powder

Synthesis

1028648-09-0

1160294-85-8

Step 1: Synthesis of 3-bromo-6,9-diphenyl-9H-carbazole In a 300 mL Erlenmeyer flask, 4.8 g (15 mmol) of 3,9-diphenyl-9H-carbazole and 250 mL of mixed solvent (ethyl acetate: toluene = 4:1) were added. The mixture was stirred for 30 min to ensure complete dissolution. Subsequently, 2.7 g (15 mmol) of N-bromosuccinimide (NBS) was slowly added and the reaction mixture was continuously stirred for 48 hours. After completion of the reaction, the reaction mixture was washed sequentially with saturated sodium bicarbonate solution and saturated brine. The organic layer was separated and dried with anhydrous magnesium sulfate. After drying, the magnesium sulfate was removed by filtration and the filtrate was concentrated to obtain an oil. A small amount of ethanol was added to the oil and the solid was induced to precipitate by ultrasonic treatment. The precipitated solid was collected by diafiltration to give 5.4 g of white powdery product in 90% yield.

References

[1] Patent: WO2009/72587, 2009, A1. Location in patent: Page/Page column 243-244
[2] Patent: TW2017/2233, 2017, A. Location in patent: Paragraph 0197; 0200; 0201
[3] Patent: WO2012/121561, 2012, A1. Location in patent: Page/Page column 26-27

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