Description

1-(2,2,2-Trifluoroethoxy)-2-ethoxyethane (CAS No. 260799-56-2) is a high-purity fluorinated ether compound with the molecular formula C₆H₁₁F₃O₂. This specialty chemical, also known by its IUPAC name 2-(2-ethoxyethoxy)-1,1,1-trifluoroethane, is designed for advanced research and industrial applications requiring fluorinated solvents or intermediates. Its unique structure combines both ethoxy and trifluoroethoxy functionalities, offering distinct physicochemical properties including enhanced thermal stability and potential low surface tension characteristics. This product is synthesized under strict quality control measures to ensure >95% purity (GC), with batch-specific certificates of analysis available. It is supplied in amber glass bottles under inert atmosphere to maintain stability, and is suitable for use in organic synthesis, material science, and specialty formulation development. Researchers investigating fluorinated compounds for electronics, coatings, or pharmaceutical applications will find this ether particularly valuable.

Properties

• CAS Number: 260799-56-2
• Complexity: 92.3
• IUPAC Name: 2-(2-ethoxyethoxy)-1,1,1-trifluoro-ethane
• InChI: InChI=1S/C6H11F3O2/c1-2-10-3-4-11-5-6(7,8)9/h2-5H2,1H3
• InChI Key: IJGQAWNPGQNIRL-UHFFFAOYSA-N
• Exact Mass: 172.07111408
• Molecular Formula: C6H11F3O2
• Molecular Weight: 172.15
• SMILES: CCOCCOCC(F)(F)F
• Topological: 18.5
• Monoisotopic Mass: 172.07111408
• Synonyms: 260799-56-2, 1-(2,2,2-Trifluoroethoxy)-2-ethoxyethane, Ethyl 2-(2,2,2-trifluoroethoxy)ethyl ether, SCHEMBL3302738, SCHEMBL3788030, SCHEMBL9871377, IJGQAWNPGQNIRL-UHFFFAOYSA-N, MFCD31694431, (2-Ethoxyethoxy)-1,1,1-trifluoroethane, 1-Ethoxy-2-(2,2,2-trifluoroethoxy)ethane, 2-(2-ethoxyethoxy)-1,1,1-trifluoroethane, H41984

Application

1-(2,2,2-Trifluoroethoxy)-2-ethoxyethane serves as a versatile fluorinated building block in synthetic organic chemistry, particularly for introducing trifluoroethoxy groups into target molecules. Its dual ether functionality makes it valuable as a specialty solvent for reactions requiring polar yet chemically stable media. Researchers utilize this compound in developing advanced materials where fluorine incorporation can modify surface properties or thermal characteristics. Potential applications include electrolyte formulations for energy storage systems and as an intermediate for pharmaceutical candidates requiring fluorine motifs.

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