2,8-DIBROMODIBENZOFURAN

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Products Intro: Product Name:2,8-Dibromodibenzofuran
CAS:10016-52-1
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CAS:10016-52-1
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Products Intro: Product Name:2,8-dibromodibenzofuran
CAS:10016-52-1
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Company Name: Shanghai Daken Advanced Materials Co.,Ltd
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Products Intro: Product Name:2,8-dibromodibenzo[b,d]furan
CAS:10016-52-1
Purity:99% Package:1KG,5KG,10KG

2,8-DIBROMODIBENZOFURAN manufacturers

  • 2,8-DIBROMODIBENZOFURAN
  • 2,8-DIBROMODIBENZOFURAN pictures
  • $50.00 / 1KG
  • 2025-09-25
  • CAS:10016-52-1
  • Min. Order: 1KG
  • Purity: 99%
  • Supply Ability: g-kg-tons, free sample is available
  • 2,8-dibromodibenzofuran
  • 2,8-dibromodibenzofuran pictures
  • $500.00 / 1KG
  • 2025-07-02
  • CAS:10016-52-1
  • Min. Order: 1KG
  • Purity: 98.0%
  • Supply Ability: 150KG /month
2,8-DIBROMODIBENZOFURAN Basic information
Product Name:2,8-DIBROMODIBENZOFURAN
Synonyms:Dibenzofuran, 2,8-dibromo-;2,8-dibroMo dibeozofuran;2,8-Dibrom-dibenzofuran;2,8-DIBROMODIBENZOFURAN;2,8-Dibromodibenzofura;2,8-dibromo-;,8-Dibromodibenzo[b,d]furan;2,8-Dibromodibenzofuran>
CAS:10016-52-1
MF:C12H6Br2O
MW:325.98
EINECS:
Product Categories:MOFS COFS;OLED
Mol File:10016-52-1.mol
2,8-DIBROMODIBENZOFURAN Structure
2,8-DIBROMODIBENZOFURAN Chemical Properties
Melting point 226℃
Boiling point 396℃
density 1.886
Fp 193℃
storage temp. Sealed in dry,Room Temperature
form powder to crystal
color White to Light yellow
InChIInChI=1S/C12H6Br2O/c13-7-1-3-11-9(5-7)10-6-8(14)2-4-12(10)15-11/h1-6H
InChIKeyUFCZRCPQBWIXTR-UHFFFAOYSA-N
SMILESO1C2=CC=C(Br)C=C2C2=CC(Br)=CC=C12
Safety Information
HS Code 2932.99.7000
MSDS Information
2,8-DIBROMODIBENZOFURAN Usage And Synthesis
Synthesis
Dibenzofuran

132-64-9

2,8-DIBROMODIBENZOFURAN

10016-52-1

General procedure for the synthesis of 2,8-dibromodibenzofuran from dibenzofuran: 1a) Synthesis of 2,8-dibromodibenzofuran: A solution of bromine (92.6 g, 0.58 mol) in acetic acid (54 g) was added slowly and dropwise at 75 °C to a solution of dibenzofuran (23.2 g, 0.14 mol) in acetic acid (232 g). The reaction mixture was stirred continuously at 75°C for 3 hours. Upon completion of the reaction, the mixture was cooled to room temperature and slowly poured into deionized water. The precipitated orange solid was washed sequentially with aqueous sodium thiosulfate and deionized water. The crude product was purified by recrystallization from n-hexane to give a white solid product in 38% yield with a melting point of 226 °C. The structure of the product was confirmed by 1H-NMR (CDCl3, ppm): 7.65 (d, 2H), 7.59 (dd, 2H), 8.03 (d, 2H).

References[1] Organic Letters, 2010, vol. 12, # 15, p. 3438 - 3441
[2] New Journal of Chemistry, 2015, vol. 39, # 3, p. 2096 - 2105
[3] Patent: WO2016/172255, 2016, A1. Location in patent: Page/Page column 101; 102
[4] Patent: KR101638767, 2016, B1. Location in patent: Paragraph 0117-0120
[5] Patent: EP2711363, 2014, A1. Location in patent: Paragraph 0252; 0253; 0254
Tag:2,8-DIBROMODIBENZOFURAN(10016-52-1) Related Product Information
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