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CAS 24079-95-6

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Ethyl 2-methyl-6-(1-methylethyl)-4-oxo-2-cyclohexene-1-carboxylate

Description:
Ethyl 2-methyl-6-(1-methylethyl)-4-oxo-2-cyclohexene-1-carboxylate, with CAS number 24079-95-6, is an organic compound characterized by its unique cyclohexene structure, which includes a carboxylate ester functional group. This compound features a cyclohexene ring that is substituted at various positions, contributing to its chemical reactivity and potential applications. The presence of the ethyl ester group enhances its solubility in organic solvents, making it useful in various chemical syntheses and formulations. Additionally, the ketone functionality (4-oxo) indicates that it may participate in reactions typical of carbonyl compounds, such as nucleophilic additions. The branched alkyl substituents (methyl and isopropyl groups) can influence the compound's steric properties and reactivity. Overall, this compound's structural characteristics suggest potential utility in organic synthesis, possibly in the development of pharmaceuticals or agrochemicals, although specific applications would depend on further research into its properties and reactivity.
Formula:C13H20O3
InChI:InChI=1S/C13H20O3/c1-5-16-13(15)12-9(4)6-10(14)7-11(12)8(2)3/h6,8,11-12H,5,7H2,1-4H3
InChI key:InChIKey=QBMOPULUXAKJTR-UHFFFAOYSA-N
SMILES:C(OCC)(=O)C1C(C(C)C)CC(=O)C=C1C
Synonyms:
  • NSC 10159
  • ethyl 2-methyl-4-oxo-6-(propan-2-yl)cyclohex-2-ene-1-carboxylate
  • Ethyl 2-methyl-6-(1-methylethyl)-4-oxo-2-cyclohexene-1-carboxylate
  • 3-Methyl-5-isopropyl-4-carbethoxy-2-cyclohexene-1-one
  • m-Menth-6-ene-2-carboxylic acid, 5-oxo-, ethyl ester (8CI)
  • Ethyl 6-(isopropyl)-2-methyl-4-oxocyclohex-2-ene-1-carboxylate
  • NSC 10159
  • AI3-06533
  • 2-Cyclohexene-1-carboxylic acid, 2-methyl-6-(1-methylethyl)-4-oxo-, ethyl ester
  • m-Menth-6-ene-2-carboxylic acid, 5-oxo-, ethyl ester
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