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Atomfair Methyl 2-fluoro-3-hydroxypropanoate C4H7FO3
Description Methyl 2-fluoro-3-hydroxypropanoate (CAS No. 671-30-7) is a high-purity fluorinated ester compound with the molecular formula C4H7FO3. This specialized chemical is widely utilized in organic synthesis, pharmaceutical research, and material science due to its unique fluorine-containing structure. The compound is supplied as a clear, colorless to pale yellow liquid with a characteristic ester odor, and is rigorously tested for purity (typically ??95% by GC analysis). Proper storage conditions (2-8??C under inert atmosphere) are recommended to maintain stability. Researchers value this reagent for its versatility as a building block in fluorinated compound synthesis and its potential applications in drug discovery programs…
Description
Description
Methyl 2-fluoro-3-hydroxypropanoate (CAS No. 671-30-7) is a high-purity fluorinated ester compound with the molecular formula C4H7FO3. This specialized chemical is widely utilized in organic synthesis, pharmaceutical research, and material science due to its unique fluorine-containing structure. The compound is supplied as a clear, colorless to pale yellow liquid with a characteristic ester odor, and is rigorously tested for purity (typically ??95% by GC analysis). Proper storage conditions (2-8??C under inert atmosphere) are recommended to maintain stability. Researchers value this reagent for its versatility as a building block in fluorinated compound synthesis and its potential applications in drug discovery programs targeting bioactive molecules.
- CAS No: 671-30-7
- Molecular Formula: C4H7FO3
- Molecular Weight: 122.09
- Exact Mass: 122.03792224
- Monoisotopic Mass: 122.03792224
- IUPAC Name: methyl 2-fluoro-3-hydroxypropanoate
- SMILES: COC(=O)C(CO)F
- Synonyms: Methyl 2-fluoro-3-hydroxypropanoate, 671-30-7, DTXSID80697093, DTXCID90647842, Methyl2-fluoro-3-hydroxypropanoate
Application
Methyl 2-fluoro-3-hydroxypropanoate serves as a key intermediate in the synthesis of fluorinated pharmaceutical compounds, particularly those targeting central nervous system disorders. The compound’s reactive hydroxyl and ester groups make it valuable for creating chiral building blocks in asymmetric synthesis. Researchers utilize this chemical in developing novel fluorinated analogs of biologically active molecules, where the fluorine atom can significantly alter metabolic stability and binding affinity. Its applications extend to materials science for creating specialized fluoropolymers with unique surface properties.
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