Identification | Back Directory | [Name]
2-bromo-3-octylthiophene | [CAS]
145543-83-5 | [Synonyms]
S1152 2-bromo-3-octylthiophene 2-BroMo-3-n-octylthiophene Thiophene,2-bromo-3-octyl- 2-Bromo-3-n-octylthiophene > 2-bromo-3-octylthiophene ISO 9001:2015 REACH | [Molecular Formula]
C12H19BrS | [MDL Number]
MFCD13193238 | [MOL File]
145543-83-5.mol | [Molecular Weight]
275.248 |
Chemical Properties | Back Directory | [Boiling point ]
123°C/1.1mmHg(lit.) | [density ]
1.206 | [refractive index ]
1.521 | [Fp ]
110℃ | [storage temp. ]
Keep in dark place,Sealed in dry,Room Temperature | [form ]
clear liquid | [color ]
Colorless to Yellow | [InChI]
InChI=1S/C12H19BrS/c1-2-3-4-5-6-7-8-11-9-10-14-12(11)13/h9-10H,2-8H2,1H3 | [InChIKey]
ISONQKSIWXLJOQ-UHFFFAOYSA-N | [SMILES]
C1(Br)SC=CC=1CCCCCCCC |
Hazard Information | Back Directory | [Chemical Properties]
Colorless to yellow to brown liquid | [Synthesis]
The synthesis of 2-bromo-3-octylthiophene (10) was carried out with reference to methods reported in the literature (He M, Leslie TM, Sinicropi JA. Synthesis of Chromophores with Exceptionally High Electro-Optic Properties. 1. Thienyl- Based Bridge Chromophores. Chem Mater 2002;14:4662-8). The procedure was as follows: 3-octylthiophene (9) (5.49 g, 28 mmol) was slowly added dropwise to a solution of N,N-dimethylformamide (DMF) (30 mL) of N-bromosuccinimide (NBS) (5.76 g, 28 mmol). The reaction mixture was stirred at room temperature for 12 hours. Upon completion of the reaction, the reaction was quenched by the addition of water (150 mL) and extracted with ethyl acetate (2 x 150 mL). The organic layers were combined, dried over anhydrous sodium sulfate, filtered and concentrated to give the crude product. The crude product was purified by n-hexane column chromatography to afford the target compound 2-bromo-3-octylthiophene (10) as a colorless oil (6.95 g, 90% yield). | [References]
[1] Patent: WO2015/15397, 2015, A1. Location in patent: Page/Page column 51 [2] Chemistry - A European Journal, 2010, vol. 16, # 6, p. 1911 - 1928 [3] Synthetic Communications, 1999, vol. 29, # 9, p. 1607 - 1610 [4] Dyes and Pigments, 2015, vol. 121, p. 99 - 108 [5] Patent: US2010/137611, 2010, A1. Location in patent: Page/Page column 14 |
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