| Weight | 128.171 g/mol |
|---|---|
| Formula | C7H12O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 4 |
Ethyl 4-pentenoate (1968-40-7)
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- A new preparation of ethyl 3-oxo-4-pentenoate: a useful annelating reagent (Journal of Organic Chemistry, 1989)
- Polymerizable tautomers, 1. Tautomerism and polymerization of ethyl 3oxo4pentenoate (Macromolecular Chemistry and Physics, 1986)
- Hydrolysis of Ethyl 4-(1-Carbethoxy-2-oxocyclopentyl)-2-pentenoate and Ethyl 4-(1-Carbethoxy-2-oxocyclopentyl)-valerate (Journal of the American Chemical Society, 1957)
- Preparative Flow Techniques; 1. Low-Temperature Organometallic Reactions: Synthesis of Ethyl 2,2-Difluoro-4-pentenoate (Synthesis, 1988)
- Polymerizable tautomers, 4. Solvent effects in radical copolymerization of ethyl 3-oxo-4-pentenoate and styrene (Macromolecular Chemistry and Physics, 1987)
- Polymerizable tautomers. VI. Solvent effects on polymerization and copolymerization of ethyl 4methyl3oxo4pentenoate (Journal of Polymer Science Part A, 1989)
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SMILESCCOC(=O)CCC=C
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Ethyl 4-pentenoate
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