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2-bromo-3-octylthiophene

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CAS:145543-83-5
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CAS:145543-83-5
Purity:98% Package:1KG;10KG;50KG

2-bromo-3-octylthiophene manufacturers

  • 2-Bromo-3-octylthiophene
  • 2-Bromo-3-octylthiophene pictures
  • $200.00 / 1KG
  • 2025-09-25
  • CAS:145543-83-5
  • Min. Order: 1KG
  • Purity: 99%, 99.5% Sublimated
  • Supply Ability: g-kg-tons, free sample is available
2-bromo-3-octylthiophene Basic information
Uses
Product Name:2-bromo-3-octylthiophene
Synonyms: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;S1152;CAS:145543-83-5;2-bromo-3-octylthiophene 98%
CAS:145543-83-5
MF:C12H19BrS
MW:275.25
EINECS:
Product Categories:Thiophene Series;Thiophenes;Building Blocks;C10 to C20+;Chemical Synthesis;Halogenated Heterocycles;Heterocyclic Building Blocks;Materials Science;Organic and Printed Electronics;Synthetic Tools and Reagents;Thiophene Monomers and Building Blocks
Mol File:145543-83-5.mol
2-bromo-3-octylthiophene Structure
2-bromo-3-octylthiophene Chemical Properties
Boiling point 123°C/1.1mmHg(lit.)
density 1.206 g/mL at 25 °C
refractive index 1.521
Fp 110℃
storage temp. Keep in dark place,Sealed in dry,Room Temperature
form clear liquid
color Colorless to Yellow
InChIInChI=1S/C12H19BrS/c1-2-3-4-5-6-7-8-11-9-10-14-12(11)13/h9-10H,2-8H2,1H3
InChIKeyISONQKSIWXLJOQ-UHFFFAOYSA-N
SMILESC1(Br)SC=CC=1CCCCCCCC
Safety Information
Safety Statements 24/25
WGK Germany 3
HS Code 29349990
Storage Class10 - Combustible liquids
MSDS Information
2-bromo-3-octylthiophene Usage And Synthesis
Uses2-Bromo-3-octylthiophene is used as an organic and pharmaceutical intermediate.
Chemical PropertiesColorless 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
2-bromo-3-octylthiophene Preparation Products And Raw materials
Raw materials3-Octylthiophene-->N-Bromosuccinimide-->N,N-Dimethylformamide
Preparation Products3,3'''-dioctyl-2,2':5',5'':2'',2'''-quaterthiophene
Tag:2-bromo-3-octylthiophene(145543-83-5) Related Product Information
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