Atomfair 2,2,3,3-Tetrafluoro-1,4-dimethoxybutane C6H10F4O2

Description 2,2,3,3-Tetrafluoro-1,4-dimethoxybutane (CAS No. 2738080-99-2) is a high-purity fluorinated ether compound with the molecular formula C6H10F4O2. This specialty chemical features a unique tetrafluoro-substituted butane backbone with terminal methoxy groups, offering exceptional thermal and chemical stability. Ideal for advanced research applications, it is supplied as a clear, colorless liquid with >98% purity (GC) and is rigorously tested for consistency. Suitable for use as a solvent, electrolyte additive, or intermediate in organic synthesis, this compound is packaged under inert gas to ensure long-term stability. Store in a cool, dry place away from strong oxidizing agents.

Description

2,2,3,3-Tetrafluoro-1,4-dimethoxybutane (CAS No. 2738080-99-2) is a high-purity fluorinated ether compound with the molecular formula C₆H₁₀F₄O₂. This specialty chemical features a unique tetrafluoro-substituted butane backbone with terminal methoxy groups, offering exceptional thermal and chemical stability. Ideal for advanced research applications, it is supplied as a clear, colorless liquid with >98% purity (GC) and is rigorously tested for consistency. Suitable for use as a solvent, electrolyte additive, or intermediate in organic synthesis, this compound is packaged under inert gas to ensure long-term stability. Store in a cool, dry place away from strong oxidizing agents.

CAS No: 2738080-99-2
Molecular Formula: C6H10F4O2
Molecular Weight: 190.14
Exact Mass: 190.06169221
Monoisotopic Mass: 190.06169221
IUPAC Name: 2,2,3,3-tetrafluoro-1,4-dimethoxybutane
SMILES: COCC(C(COC)(F)F)(F)F
Synonyms: 2,2,3,3-tetrafluoro-1,4-dimethoxybutane, 2738080-99-2, 888-093-1, MFCD32876892, 4,4,5,5-Tetrafluoro-2,7-dioxaoctane

Application

2,2,3,3-Tetrafluoro-1,4-dimethoxybutane is primarily used as a fluorinated solvent or co-solvent in lithium-ion battery electrolytes to enhance thermal stability and electrochemical performance. Its unique structure also makes it a valuable building block for synthesizing fluorinated polymers or surfactants with tailored hydrophobicity. Researchers may employ it as a specialty reagent in nucleophilic substitution reactions or as a precursor for advanced material science applications.

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