Description
3-[2-(2-Ethoxyethoxy)ethoxy]thiophene (CAS No. 138625-91-9) is a high-purity organic compound with the molecular formula C10H16O3S. This specialized thiophene derivative features a unique ethoxyethoxyethoxy side chain, enhancing its solubility and reactivity for advanced synthetic applications. Ideal for researchers in materials science, organic electronics, and polymer chemistry, this compound serves as a versatile building block for conductive polymers, organic semiconductors, and functionalized heterocycles. Its well-defined structure ensures consistency in polymerization and modification reactions. Packaged under inert conditions to maintain stability, this product is rigorously tested for purity (typically ≥95% by GC or HPLC) and is available in scalable quantities for both lab-scale and industrial applications.
Properties
- CAS Number: 138625-91-9
- Complexity: 133
- IUPAC Name: 3-[2-(2-ethoxyethoxy)ethoxy]thiophene
- InChI: InChI=1S/C10H16O3S/c1-2-11-4-5-12-6-7-13-10-3-8-14-9-10/h3,8-9H,2,4-7H2,1H3
- InChI Key: ZVDPUBPRSFKMAI-UHFFFAOYSA-N
- Exact Mass: 216.08201554
- Molecular Formula: C10H16O3S
- Molecular Weight: 216.30
- SMILES: CCOCCOCCOC1=CSC=C1
- Topological: 55.9
- Monoisotopic Mass: 216.08201554
- Synonyms: 138625-91-9, Thiophene, 3-[2-(2-ethoxyethoxy)ethoxy]-, 3-[2-(2-ETHOXYETHOXY)ETHOXY]THIOPHENE, DTXSID10769116, Thiophene,3-[2-(2-ethoxyethoxy)ethoxy]-
Application
3-[2-(2-Ethoxyethoxy)ethoxy]thiophene is widely used as a monomer for synthesizing conductive polymers, particularly in the development of organic electronic devices such as OLEDs and thin-film transistors. Its flexible side chain improves processability in solution-based polymerizations. Researchers also employ it as a precursor for functionalized thiophene derivatives in photovoltaic materials. The compound’s electron-rich thiophene core makes it valuable for designing charge-transport materials in energy storage systems.
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