| Weight | 114.144 g/mol |
|---|---|
| Formula | C6H10O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 2 |
ETHYL CROTONATE (623-70-1, 10544-63-5)
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- Sigma-Aldrich - ETHYL CROTONATE38.30 - 556.00 USD
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- Deconjugative alkylation of the enolate anion derived from ethyl crotonate (Tetrahedron Letters, 1973)
- Stereochemistry of nucleophilic conjugate addition. Addition of ethanol-d and 2-methyl-2-propanethiol-d to ethyl crotonate (Journal of the American Chemical Society, 1990)
- Gas-phase oxidation of methyl crotonate and ethyl crotonate. kinetic study of their reactions toward OH radicals and Cl atoms. (Journal of Physical Chemistry A, 2012)
- The Peroxide Effect in the Addition of Reagents to Unsaturated Substances. XXII. The Addition of Hydrogen Bromide to Trimethylethylene, Styrene, Crotonic Acid, and Ethyl Crotonate (Journal of the American Chemical Society, 1939)
- RADIATION AND ULTRAVIOLET INDUCED ADDITION OF ALCOHOLS TO ETHYL CROTONATE. (Journal of Organic Chemistry, 1972)
- The Synthesis of Pyrrolizidines. III. Condensation of Nitromethane with Ethyl Crotonate and Subsequent Formation of 1-Methylpyrrolizidine (Heliotridane, Pseudoheliotridane) (Journal of the American Chemical Society, 1949)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCCOC(=O)C=CC
-
InChIKeyZFDIRQKJPRINOQ-UHFFFAOYSA-N
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Synthesis
Reactant
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
Reactant
+
1-Hydroxy-1,2-benziodoxol-3(1H)-one 1-oxide
(Nicolaou IBX dehydrogenation)
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ETHYL CROTONATE
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