| Weight | 164.588 g/mol |
|---|---|
| Formula | C6H9ClO3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 3 |
Ethyl 2-chloroacetoacetate (609-15-4)
A 21960 · A-21960
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- Fungal Aerobic Reductive Dechlorination of Ethyl 2Chloroacetoacetate by Saccharomyces cerevisiae: Mechanism of a Novel Type of Microbial Dehalogenation (ChemBioChem, 2004)
- An unexpected result in the condensation of 2amino6bromopyridine with ethyl 4chloroacetoacetate: Four dihalosubstituted pyrido[1,2a]pyrimidin4ones as reaction products (Journal of Heterocyclic Chemistry, 1999)
- Selective synthesis of oxygen-containing heterocycles via tandem reactions of 1,2-allenic ketones with ethyl 4-chloroacetoacetate (RSC Advances, 2013)
- Chlorine DioxideIodineEthyl 2-Chloroacetoacetate Oscillation Reaction Investigated by UVVis and Online FTIR Spectrophotometric Methods (Journal of Solution Chemistry, 2014)
- The Reaction of Ethyl 2-Chloroacetoacetate with 2-(Alkylamino) Alcohols: an Unexpected Formation of the 2-Methyloxazolidine Ring (Journal of Chemical Research-s, 1998)
- Synthesis of 2-chloro-3-oxoesters by reaction of the dianion of ethyl 2-chloroacetoacetate with electrophiles (Monatshefte Fur Chemie, 2013)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - A 21960
- A-21960
-
SMILESCCOC(=O)C(C(=O)C)Cl
-
InChIKeyRDULEYWUGKOCMR-UHFFFAOYSA-N
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Alternate Names
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Synthesis
Reactant
+
Ethanol
(O-acylation)
Reactant
+
Chloroethane
(Ester from carboxilic acid(SN2))
Reactant
+
CARBON TETRACHLORIDE
(Appel reaction)
Reactant
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
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Ethyl 2-chloroacetoacetate
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