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  • 515493 - 5,5′-Dibromo-2,2′-bithiophene

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515493 Sigma-Aldrich

5,5′-Dibromo-2,2′-bithiophene

99%

  • CAS Number 4805-22-5

  • Empirical Formula (Hill Notation) C8H4Br2S2

  • Molecular Weight 324.06

  •  MDL number MFCD00219110

  •  PubChem Substance ID 24873824

  •  NACRES NA.23

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Properties

Related Categories Building Blocks, C7 to C9, Chemical Synthesis, Halogenated Heterocycles, Heterocyclic Building Blocks,
assay   99%
mp   144-146 °C (lit.)
SMILES string   Brc1ccc(s1)-c2ccc(Br)s2
InChI   1S/C8H4Br2S2/c9-7-3-1-5(11-7)6-2-4-8(10)12-6/h1-4H
InChI key   SXNCMLQAQIGJDO-UHFFFAOYSA-N

Description

Packaging

1, 5 g in glass bottle

Safety & Documentation

Safety Information

Personal Protective Equipment 
RIDADR 
NONH for all modes of transport
WGK Germany 
WGK 3
Flash Point(F) 
Not applicable
Flash Point(C) 
Not applicable

Documents

Certificate of Analysis (COA)

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Protocols & Articles

Articles

Organic Bioelectronic Materials and Devices for Bridging Biology and Traditional Electronics

1 Department of Biomedical Engineering, Northwestern University, Evanston, IL 60208, USA 2 Simpson Querrey Institute for BioNanotechnology, Northwestern University, Chicago, IL 60611, USA 3 Departmen...
Keywords: Adhesion, Amplification, Bacterial conjugations, C-C bond formation, Coupling reactions, Diffusion, Electronics, Microelectronics, Nanotubes, Neurotransmitters, Polymerization reactions, Reductions, Semiconductor, Solvents, Transduction

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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

Peer-Reviewed Papers
15

References

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