Atomfair Carbonic acid, 2-fluoroethyl methyl ester C4H7FO3

Description 2-Fluoroethyl Methyl Carbonate (CAS No. 659718-69-1) is a high-purity fluorinated carbonate ester with the molecular formula C4H7FO3. This specialized chemical is designed for advanced research and industrial applications, particularly in the fields of electrolyte formulation and organic synthesis. Its unique fluorinated structure enhances electrochemical stability, making it a valuable candidate for lithium-ion battery electrolytes. The compound is rigorously tested for purity and consistency, ensuring reliable performance in sensitive applications. Available in various quantities, it is packaged under inert conditions to maintain stability and shelf life.

Description

2-Fluoroethyl Methyl Carbonate (CAS No. 659718-69-1) is a high-purity fluorinated carbonate ester with the molecular formula C₄H₇FO₃. This specialized chemical is designed for advanced research and industrial applications, particularly in the fields of electrolyte formulation and organic synthesis. Its unique fluorinated structure enhances electrochemical stability, making it a valuable candidate for lithium-ion battery electrolytes. The compound is rigorously tested for purity and consistency, ensuring reliable performance in sensitive applications. Available in various quantities, it is packaged under inert conditions to maintain stability and shelf life.

CAS No: 659718-69-1
Molecular Formula: C4H7FO3
Molecular Weight: 122.09
Exact Mass: 122.03792224
Monoisotopic Mass: 122.03792224
IUPAC Name: 2-fluoroethyl methyl carbonate
SMILES: COC(=O)OCCF
Synonyms: Carbonic acid, 2-fluoroethyl methyl ester, 659718-69-1, SCHEMBL320782

Application

2-Fluoroethyl Methyl Carbonate is primarily used as a fluorinated solvent or co-solvent in lithium-ion battery electrolytes, where it improves thermal and electrochemical stability. Researchers also explore its potential as a building block in organic synthesis for pharmaceuticals and agrochemicals. Its fluorinated moiety offers unique reactivity in nucleophilic substitution reactions.

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