| Weight | 170.208 g/mol |
|---|---|
| Formula | C9H14O3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 2 |
Ethyl 2-oxocyclohexanecarboxylate (1655-07-8)
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- Sigma-Aldrich - Ethyl 2-oxocyclohexanecarboxylate89.70 - 220.50 USD
- Fisher Scientific - Search for Ethyl 2-oxocyclohexanecarboxylate
- TCI - Ethyl 2-oxocyclohexanecarboxylate65.00 - 662.00 USD
- Enantioselective synthesis of the hexahydronaphthalene nucleus of (-)-compactin from ethyl (1R,2S)-2-methyl-4-oxocyclohexanecarboxylate and 2-(3-nitropropyl)-1,3-dioxolane as four carbon bifunctional annelating agent (Tetrahedron, 1994)
- Synthesis of ()-Nitramine and ()-Isonitramine by Utilizing Stereoselective Reduction of Ethyl 1-(3-Bromopropyl)-2-oxocyclohexanecarboxylate (Heterocycles, 1997)
- The CArylation of Dicarbonyl Compounds: Ethyl 1(pMethoxyphenyl)2Oxocyclohexanecarboxylate (Organic Syntheses, 2003)
- ChemInform Abstract: Synthesis of (.+-.)-Nitramine and (.+-.)-Isonitramine by Utilizing Stereoselective Reduction of Ethyl 1-(3-Bromopropyl)-2-oxocyclohexanecarboxylate. (ChemInform, 2010)
- ChemInform Abstract: Enantioselective Synthesis of the Hexahydronaphthalene Nucleus (XIII) of ()Compactin from Ethyl (1R,2S)2Methyl4 oxocyclohexanecarboxylate and 2(3Nitropropyl)1,3dioxolane as Four Carbon Bifunctional Annelating Agent. (ChemInform, 2010)
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Predict GHS Hazards for Any Chemical in silico.
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SMILESCCOC(=O)C1CCCCC1=O
-
InChIKeyFGSGHBPKHFDJOP-UHFFFAOYSA-N
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Synthesis
Reactant
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
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Ethyl 2-oxocyclohexanecarboxylate
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