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ChemicalBook--->CAS DataBase List--->1089687-05-7

1089687-05-7

1089687-05-7 Structure

1089687-05-7 Structure
IdentificationBack Directory
[Name]

2,6-Dibromo-4,4-bis(2-ethylhexyl)-4H-silolo[3,2-b:4,5-b']dithiophene
[CAS]

1089687-05-7
[Synonyms]

DTS26-2Br
2,6-Dibromo-4,4-bis(2-ethylhexyl)-4H-silolo[3,2-b
4,4'-Bis(2-ethyl-hexyl)-5,5'-dibroMo-dithieno[3,2-b:2',3'-d
2,6‐dibroMo‐(4,4‐di‐2‐ ethylhexyldithieno[ 3,2‐b:2',3'‐ d]silole
4,4'-Bis(2-ethyl-hexyl)-5,5'-dibroMo-dithieno[3,2-b:2',3'-d]silole
2,6-Dibromo-4,4-bis(2-ethylhexyl)-4H-silolo[3,2-b:4,5-b']dithiophene
4H-Silolo[3,2-b:4,5-b']dithiophene, 2,6-dibroMo-4,4-bis(2-ethylhexyl)-
2,6-Dibromo-4,4-bis(2-ethylhexyl)-4H-silolo[3,2-b:4,5-b']dithiophene
2,6-Dibromo-4,4-bis(2-ethylhexyl)-4H-thieno[2',3':4,5]silolo[3,2- b]thiophene
[EINECS(EC#)]

200-258-5
[Molecular Formula]

C24H36Br2S2Si
[MDL Number]

MFCD16621138
[MOL File]

1089687-05-7.mol
[Molecular Weight]

576.57
Chemical PropertiesBack Directory
[Boiling point ]

551.3±50.0 °C(Predicted)
[density ]

1.32
[storage temp. ]

Keep in dark place,Inert atmosphere,2-8°C
[InChI]

InChI=1S/C24H36Br2S2Si/c1-5-9-11-17(7-3)15-29(16-18(8-4)12-10-6-2)19-13-21(25)27-23(19)24-20(29)14-22(26)28-24/h13-14,17-18H,5-12,15-16H2,1-4H3
[InChIKey]

CMMVJTQAECTXDZ-UHFFFAOYSA-N
[SMILES]

C12C3SC(Br)=CC=3[Si](CC(CC)CCCC)(CC(CC)CCCC)C=1C=C(Br)S2
Hazard InformationBack Directory
[Synthesis]

4H-Silolo[3,2-b:4,5-b']dithiophene, 4,4-bis(2-ethylhexyl)-2,6-bis(trimethylsilyl)-

1089687-04-6

2,6-Dibromo-4,4-bis(2-ethylhexyl)-4H-silolo[3,2-b:4,5-b']dithiophene

1089687-05-7

The general procedure for the synthesis of 2,6-dibromo-4,4-bis(2-ethylhexyl)-4H-silacyclopenta[3,2-B:4,5-B']dithiophene, using the compound (CAS:1089687-04-6) as a starting material, was as follows: at 10 °C, N-bromosuccinimide (NBS) (11.65 g, 65.42 mmol. 2.06 eq.) was slowly added to a solution of the compound (17.885 g, 31.76 mmol) dissolved in 350 ml of anhydrous tetrahydrofuran. The reaction mixture was stirred at room temperature overnight. Upon completion of the reaction, the crude product was purified by silica gel column chromatography (eluent: n-hexane) to afford the target compound 17a (16.47 g, 90% yield) as a yellow oil.

[References]

[1] Journal of the American Chemical Society, 2008, vol. 130, # 48, p. 16144 - 16145
[2] Chemical Communications, 2009, # 37, p. 5570 - 5572
[3] Patent: KR2017/50088, 2017, A. Location in patent: Paragraph 0237; 0238
[4] Patent: EP2530085, 2012, A1. Location in patent: Page/Page column 11-12
[5] Organic Electronics: physics, materials, applications, 2016, vol. 39, p. 361 - 370
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