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Atomfair 1,1-Difluoro-2-(2-fluoroethoxy)ethane C4H7F3O
Description 1,1-Difluoro-2-(2-fluoroethoxy)ethane (CAS No. 2708335-42-4) is a high-purity fluorinated ether compound with the molecular formula C4H7F3O . This specialty chemical is designed for advanced research and industrial applications, offering exceptional stability and reactivity due to its unique fluorine substitution pattern. The IUPAC name, 1,1-difluoro-2-(2-fluoroethoxy)ethane , reflects its precise molecular structure, which features a difluoroethyl group linked to a fluoroethoxy moiety. Available in rigorously controlled batches, this compound is ideal for organofluorine chemistry, electrolyte formulation, and materials science research. Each shipment includes comprehensive analytical data (GC/MS, NMR) to ensure reproducibility and quality for sensitive applications.
Description
Description
1,1-Difluoro-2-(2-fluoroethoxy)ethane (CAS No. 2708335-42-4) is a high-purity fluorinated ether compound with the molecular formula C4H7F3O. This specialty chemical is designed for advanced research and industrial applications, offering exceptional stability and reactivity due to its unique fluorine substitution pattern. The IUPAC name, 1,1-difluoro-2-(2-fluoroethoxy)ethane, reflects its precise molecular structure, which features a difluoroethyl group linked to a fluoroethoxy moiety. Available in rigorously controlled batches, this compound is ideal for organofluorine chemistry, electrolyte formulation, and materials science research. Each shipment includes comprehensive analytical data (GC/MS, NMR) to ensure reproducibility and quality for sensitive applications.
- CAS No: 2708335-42-4
- Molecular Formula: C4H7F3O
- Molecular Weight: 128.09
- Exact Mass: 128.04489933
- Monoisotopic Mass: 128.04489933
- IUPAC Name: 1,1-difluoro-2-(2-fluoroethoxy)ethane
- SMILES: C(CF)OCC(F)F
- Synonyms: SCHEMBL15661347, MFCD35255448, 2708335-42-4
Application
1,1-Difluoro-2-(2-fluoroethoxy)ethane serves as a versatile building block in fluorinated electrolyte systems for next-generation lithium-ion batteries, where its structural properties enhance ionic conductivity and thermal stability. Researchers utilize it as a precursor in the synthesis of fluorinated polymers and surfactants with tailored hydrophobicity and chemical resistance. The compound’s fluoroether linkage also makes it valuable in pharmaceutical intermediate development for metabolic stability studies.
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