Description
Ethyl 2-fluoro-3-oxopentanoate (CAS No. 759-67-1) is a high-purity fluorinated ester compound with the molecular formula C7H11FO3. This specialty chemical is widely utilized in organic synthesis, pharmaceutical research, and agrochemical development due to its reactive keto-ester and fluorine functionalities. The compound is supplied as a clear to pale-yellow liquid with >95% purity (GC), ensuring consistency for demanding applications. Its IUPAC name, ethyl 2-fluoro-3-oxopentanoate, reflects the precise molecular structure featuring an ethyl ester group adjacent to both fluorine and ketone moieties. Proper storage at 2-8°C under inert atmosphere is recommended to maintain stability. Available in research quantities (100mg to 5kg) with optional custom packaging.
Properties
- CAS Number: 759-67-1
- Complexity: 156
- IUPAC Name: ethyl 2-fluoro-3-oxo-pentanoate
- InChI: InChI=1S/C7H11FO3/c1-3-5(9)6(8)7(10)11-4-2/h6H,3-4H2,1-2H3
- InChI Key: ODPHSEIVAPWGAZ-UHFFFAOYSA-N
- Exact Mass: 162.06922237
- Molecular Formula: C7H11FO3
- Molecular Weight: 162.16
- SMILES: CCC(=O)C(C(=O)OCC)F
- Topological: 43.4
- Monoisotopic Mass: 162.06922237
- Synonyms: Ethyl 2-fluoro-3-oxopentanoate, 759-67-1, DTXSID30545257, DTXCID20496042, 2-fluoro-3-oxopentanoic acid ethylester, 2-fluoro-3-oxopentanoic acid ethyl ester, 2-Fluoro-3-oxo-pentanoic acid ethyl ester, Ethyl2-fluoro-3-oxopentanoate, C7H11FO3, MFCD09753153, SCHEMBL3782518, AKOS005063661, AS-15051, DB-001225, EN300-93353, E78287
Application
Ethyl 2-fluoro-3-oxopentanoate serves as a versatile building block in medicinal chemistry, particularly for introducing fluorine atoms into target molecules. Researchers employ this compound in the synthesis of fluorinated heterocycles and bioactive intermediates. The reactive β-keto ester moiety enables facile condensation reactions, while the fluorine substituent modulates electronic properties. Applications extend to materials science where it functions as a precursor for specialty fluoropolymers.
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