| Weight | 170.208 g/mol |
|---|---|
| Formula | C9H14O3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 2 |
Ethyl 3-oxocyclohexanecarboxylate (33668-25-6)
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Most-cited Publications
- 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)
- 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)
Trends
Alternate Names
-
SMILESCCOC(=O)C1CCCC(=O)C1
-
InChIKeyYLRVJPQVDQQBOX-UHFFFAOYSA-N
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LabBot found multiple suppliers for 
Ethyl 3-oxocyclohexanecarboxylate
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