Description
2,5-Bis(2-ethylhexyl)thiophene (CAS No. 1415929-75-7) is a high-purity organic compound with the molecular formula C20H36S, widely utilized in advanced material research and specialty chemical synthesis. This thiophene derivative features two 2-ethylhexyl substituents at the 2 and 5 positions, enhancing its solubility in organic solvents and compatibility with polymer matrices. Ideal for applications in organic electronics, it serves as a key building block for conductive polymers, organic semiconductors, and photovoltaic materials. Our product is rigorously tested for consistency, ensuring optimal performance in sensitive research environments. Available in various quantities, it is packaged under inert conditions to maintain stability and purity.
Properties
- CAS Number: 1415929-75-7
- Complexity: 214
- IUPAC Name: 2,5-bis(2-ethylhexyl)thiophene
- InChI: InChI=1S/C20H36S/c1-5-9-11-17(7-3)15-19-13-14-20(21-19)16-18(8-4)12-10-6-2/h13-14,17-18H,5-12,15-16H2,1-4H3
- InChI Key: HPMWIVUDOOWKGX-UHFFFAOYSA-N
- Exact Mass: 308.25377232
- Molecular Formula: C20H36S
- Molecular Weight: 308.6
- SMILES: CCCCC(CC)CC1=CC=C(S1)CC(CC)CCCC
- Topological: 28.2
- Monoisotopic Mass: 308.25377232
- Synonyms: 2,5-Bis(2-ethylhexyl)thiophene, 1415929-75-7, SCHEMBL18066726
Application
2,5-Bis(2-ethylhexyl)thiophene is primarily employed in the development of conjugated polymers for organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its extended alkyl chains improve processability and film-forming properties in solution-processed electronic devices. Researchers also utilize it as a monomer for synthesizing polythiophene derivatives with tailored optoelectronic characteristics. Additionally, it finds use in dye-sensitized solar cells (DSSCs) and as a dopant for enhancing charge transport in thin-film devices.
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