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Atomfair Diethyl fluoromalonate C7H11FO4
Description Diethyl Fluoromalonate (CAS 685-88-1) is a highly versatile fluorinated malonate ester with the molecular formula C7H11FO4. This compound, also known by its IUPAC name diethyl 2-fluoropropanedioate , is a clear to pale yellow liquid widely used in organic synthesis and pharmaceutical research. Its unique fluorinated structure makes it a valuable building block for the preparation of fluorinated heterocycles, agrochemicals, and bioactive molecules. With a purity of ??98%, our Diethyl Fluoromalonate is rigorously tested via GC, NMR, and HPLC to ensure consistency for sensitive applications. It is supplied in amber glass bottles under inert gas to maintain stability and is…
Description
Description
Diethyl Fluoromalonate (CAS 685-88-1) is a highly versatile fluorinated malonate ester with the molecular formula C7H11FO4. This compound, also known by its IUPAC name diethyl 2-fluoropropanedioate, is a clear to pale yellow liquid widely used in organic synthesis and pharmaceutical research. Its unique fluorinated structure makes it a valuable building block for the preparation of fluorinated heterocycles, agrochemicals, and bioactive molecules. With a purity of ??98%, our Diethyl Fluoromalonate is rigorously tested via GC, NMR, and HPLC to ensure consistency for sensitive applications. It is supplied in amber glass bottles under inert gas to maintain stability and is suitable for use in nucleophilic fluorination reactions, cross-coupling reactions, and as a precursor for fluorinated intermediates. Store in a cool, dry place away from oxidizing agents.
- CAS No: 685-88-1
- Molecular Formula: C7H11FO4
- Molecular Weight: 178.16
- Exact Mass: 178.06413699
- Monoisotopic Mass: 178.06413699
- IUPAC Name: diethyl 2-fluoropropanedioate
- SMILES: CCOC(=O)C(C(=O)OCC)F
- Synonyms: Diethyl fluoromalonate, Diethyl 2-fluoromalonate, Fluoromalonic acid diethyl ester, Diethyl fluoropropanedioate, Propanedioic acid, fluoro-, diethyl ester
Application
Diethyl Fluoromalonate is widely employed as a key fluorinated synthon in pharmaceutical and agrochemical research, particularly in the synthesis of fluorinated analogs of biologically active compounds. It serves as a precursor for the preparation of fluorinated heterocycles and specialty chemicals via nucleophilic substitution or condensation reactions. Researchers also utilize it in the development of fluorinated polymers and materials with tailored properties.
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