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2,7-Dibromo-9,10-phenanthrenedione

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2,7-Dibromo-9,10-phenanthrenedione Basic information

Product Name:
2,7-Dibromo-9,10-phenanthrenedione
Synonyms:
  • 2,7-DIBROMO-9,10-PHENANTHRENEDIONE
  • 2,7-dibromo-phenanthrene-9,10-dione
  • 2,7-Dibromo-9,10-phenanthrenequinone
  • 2,7-dibroMo-9,10-dihydrophenanthrene-9,10-dione
  • 1g/2100
  • 2,7-DibroMo-9,10-Dihydrophenanthrene-9,10-Dione,2,7-Dibromo-9,10-Phenanthrenequinone
  • 2,7-Dibromo-9,10-phenanthren
  • JACS-84405-44-7
CAS:
84405-44-7
MF:
C14H6Br2O2
MW:
366
EINECS:
805-819-4
Product Categories:
  • Naphthyridine,Quinoline
  • Electronic Chemicals
  • OLED
Mol File:
84405-44-7.mol
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2,7-Dibromo-9,10-phenanthrenedione Chemical Properties

Melting point:
331°C(lit.)
Boiling point:
503.8±43.0 °C(Predicted)
Density 
1.911±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
form 
powder to crystal
color 
Light yellow to Yellow to Orange
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Safety Information

HS Code 
2914790090
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2,7-Dibromo-9,10-phenanthrenedione Usage And Synthesis

Chemical Properties

light yellow solid

Uses

2,7-Dibromophenanthrene-9,10-dione is used as a modifier in solar cells.

Synthesis

84-11-7

84405-44-7

The general procedure for the synthesis of 2,7-dibromo-9,10-phenanthrenequinone from phenanthrenequinone is as follows: Example 1: Synthesis of 6,11-bis(phenoxazin-10-yl)-1,4-diazabenzophenanthrene (Compound 1) 1. 9,10-phenanthrenequinone (10 g) and concentrated sulfuric acid (100 mL) were added to a dry reaction vessel under nitrogen protection. 2. N-bromosuccinimide (18 g) was added to the reaction mixture and the reaction was stirred for 2 hours at room temperature. 3. Upon completion of the reaction, the reaction was quenched by the slow addition of water (50 mL), followed by pouring the mixture into ice water (600 mL). 4. The precipitated solid product was collected by filtration and washed with hot water. 5. The crude product was extracted by refluxing with ethyl acetate (100 mL) and then vacuum dried to give 2,7-dibromo-9,10-phenanthrenequinone as a yellow solid in 73% yield.

References

[1] Chemical Communications, 2014, vol. 50, # 32, p. 4172 - 4174
[2] Patent: US2005/176952, 2005, A1. Location in patent: Page/Page column 5
[3] Patent: CN107400129, 2017, A. Location in patent: Paragraph 0113-0114
[4] Organic Letters, 2012, vol. 14, # 10, p. 2564 - 2567
[5] Journal of Polymer Science, Part A: Polymer Chemistry, 2010, vol. 48, # 8, p. 1714 - 1720

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