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739375 Sigma-Aldrich

5-Bromo-5′-hexyl-2,2′-bithiophene

98%

Synonym: 2-(5-Bromothiophen-2-yl)-5-hexylthiophene

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Description

Packaging

1, 5 g in glass bottle

Safety & Documentation

Safety Information

Symbol 
GHS06  GHS06
Signal word 
Danger
Hazard statements 
Precautionary statements 
RIDADR 
UN 2811 6.1 / PGIII
WGK Germany 
3
Flash Point(F) 
>230 °F
Flash Point(C) 
>110 °C

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Protocols & Articles

Articles

Development of Organic Semiconductors from Highly Ordered Oligo and Polythiophenes

Nicholas S. Colella, Lei Zhang, Alejandro L. Briseño* Polymer Science & Engineering Department, University of Massachusetts, Amherst, Massachusetts 01003 *Email: abriseno@mail.pse.umass.edu
Keywords: Absorption, Building blocks, Catalysis, Coupling reactions, Cross couplings, Crystallization, Electronics, Environmental, Grignard Reaction, Metathesis, Nanomaterials, Nucleic acid annealing, Organic electronics, Photovoltaics, Polymer science, Polymerization reactions, Semiconductor, Solar cells, Ultraviolet-Visible spectroscopy

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Oligothiophene Synthesis

Oligothiophenes and their functional derivatives are used in a number of high-technology applications including OLEDs, OFETs and OPVs, where the ability to functionalize the oligothiophene backbone a...
Keywords: Building blocks, Coupling reactions, Sublimation, Suzuki coupling

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