ChemicalBook--->CAS DataBase List--->145543-83-5

145543-83-5

145543-83-5 Structure

145543-83-5 Structure
IdentificationBack 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 PropertiesBack 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
Questions And AnswerBack Directory
[Uses]

2-Bromo-3-octylthiophene is used as an organic and pharmaceutical intermediate.
Safety DataBack Directory
[Symbol(GHS) ]

Corrosion (GHS05)Exclamation Mark (GHS07)Health Hazard (GHS08)
GHS05,GHS07,GHS08
[Signal word ]

Warning
[Hazard statements ]

H413
[Precautionary statements ]

P501-P273
[Safety Statements ]

24/25
[WGK Germany ]

3
[HS Code ]

29349990
[Storage Class]

10 - Combustible liquids
Hazard InformationBack Directory
[Chemical Properties]

Colorless to yellow to brown liquid
[Synthesis]

3-Octylthiophene

65016-62-8

2-bromo-3-octylthiophene

145543-83-5

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
Spectrum DetailBack Directory
[Spectrum Detail]

2-bromo-3-octylthiophene(145543-83-5)1HNMR
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