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Energy Chemical |
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400-0056266 |
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| Company Name: |
Sigma-Aldrich |
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| | Ethyl 4-methyl-2-cyclohexanone-1-carboxylate Basic information |
| | Ethyl 4-methyl-2-cyclohexanone-1-carboxylate Chemical Properties |
| Melting point | 53-54 °C | | Boiling point | 128-132 °C/32 mmHg (lit.) | | density | 1.045 g/mL at 25 °C (lit.) | | vapor pressure | 28Pa at 25℃ | | refractive index | n20/D 1.473(lit.) | | Fp | >230 °F | | pka | 12.09±0.40(Predicted) | | Water Solubility | 2.56g/L at 20℃ | | InChI | 1S/C10H16O3/c1-3-13-10(12)8-5-4-7(2)6-9(8)11/h7-8H,3-6H2,1-2H3 | | InChIKey | FFVHHWOJYFCNJP-UHFFFAOYSA-N | | SMILES | CCOC(=O)C1CCC(C)CC1=O | | LogP | 4.36 at 30℃ |
| WGK Germany | 3 | | HS Code | 2918300090 | | Storage Class | 10 - Combustible liquids |
| | Ethyl 4-methyl-2-cyclohexanone-1-carboxylate Usage And Synthesis |
| Uses | Reactant involved in:• ;Hydroxylation / oxidative chlorination with hydrogen peroxide1• ;Heterocyclization2• ;Cyclization of generated dianions followed by dehydrogenation3• ;Palladium-catalyzed isomerization4• ;Regioselective cyclizations5• ;Vinylogous Michael reactions6 | | Uses | 2-Carbethoxy-5-methylcyclohexanone is a useful chemical reagent in organic synthesis. It is reported that 2-Carbethoxy-5-methylcyclohexanone is used in the synthesis of optically active α-methylene γ-butyrolactones and (+)-mintlactone. | | Uses | Reactant involved in:
- Hydroxylation / oxidative chlorination with hydrogen peroxide
- Heterocyclization
- Cyclization of generated dianions followed by dehydrogenation
- Palladium-catalyzed isomerization
- Regioselective cyclizations
- Vinylogous Michael reactions
| | Flammability and Explosibility | Not classified |
| | Ethyl 4-methyl-2-cyclohexanone-1-carboxylate Preparation Products And Raw materials |
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