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