Basic information Safety Supplier Related

2,6-Dibromodithieno[3,2-b:2',3'-d]thiophene

Basic information Safety Supplier Related

2,6-Dibromodithieno[3,2-b:2',3'-d]thiophene Basic information

Product Name:
2,6-Dibromodithieno[3,2-b:2',3'-d]thiophene
Synonyms:
  • 2,6-Dibromodithieno[3,2-b:2',3'-d]thiophene
  • 2,6-DibroMo-dithieno[3,2-b
  • 26-dibromobisthieno[32-b23-d]thiophene
  • 2,6-dibromodithieno[2,3-a:2',3'-d]thiophene
  • 2,6-Dibromodithieno[3,2-b:2',3'-d]thiophene>
  • Dithieno[3,2-b:2',3'-d]thiophene, 2,6-dibromo-
  • M8806
  • TTT-2Br
CAS:
67061-69-2
MF:
C8H2Br2S3
MW:
354.1
Mol File:
67061-69-2.mol
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2,6-Dibromodithieno[3,2-b:2',3'-d]thiophene Chemical Properties

Melting point:
171℃ (chloroform methanol )
Boiling point:
447.9±40.0 °C(Predicted)
Density 
2.234±0.06 g/cm3(Predicted)
storage temp. 
2-8°C
solubility 
soluble in Toluene
form 
powder to crystal
color 
White to Light yellow to Green
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Safety Information

Hazard Codes 
Xn
Risk Statements 
22-36
Safety Statements 
26
WGK Germany 
3
HS Code 
29349990
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2,6-Dibromodithieno[3,2-b:2',3'-d]thiophene Usage And Synthesis

Chemical Properties

White to yellow to tan solid

Synthesis

3593-75-7

67061-69-2

General procedure for the synthesis of 2,5-dibromodithieno[3,2-B:2',3'-D]thiophene using dithieno[3,2-B:2',3'-D]thiophene as starting material: at 0 °C, N-bromosuccinimide (5.87 g, 33 mmol) was slowly added to dithieno[3,2-B:2',3'-D]thiophene (Aldrich, 2.94 g, 2.94 g, 2.94 g, 1.5 mmol) dissolved in an anhydrous DMF (60 mL). 15 mmol) was dissolved in a solution of anhydrous DMF (60 mL). The reaction mixture was gradually warmed to room temperature and stirred overnight. Subsequently, the reaction solution was poured into water and the precipitate precipitated was collected. The precipitate was washed with methanol and recrystallized in a chloroform/methanol solvent mixture to finally obtain off-white crystals of 2,5-dibromodithieno[3,2-B:2',3'-D]thiophene (yield: 5.14 g, 97%).1H NMR (500 MHz, CDCl3): δ 7.28 (s, 2H).

References

[1] Journal of Materials Chemistry, 2012, vol. 22, # 33, p. 16810 - 16816
[2] Patent: US2013/207081, 2013, A1. Location in patent: Paragraph 0081; 0082; 0083
[3] Angewandte Chemie - International Edition, 2015, vol. 54, # 9, p. 2734 - 2738
[4] Angew. Chem., 2015, vol. 127, # 9, p. 2772 - 2776,5
[5] Patent: CN105646528, 2016, A. Location in patent: Paragraph 0069; 0070

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