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CAS 487-34-3

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2,6-Piperidinedione, 4-[2-(3,5-dimethyl-6-oxo-1-cyclohexen-1-yl)-2-hydroxyethyl]- (9CI)

Description:
2,6-Piperidinedione, 4-[2-(3,5-dimethyl-6-oxo-1-cyclohexen-1-yl)-2-hydroxyethyl]- (CAS 487-34-3) is a chemical compound characterized by its piperidine ring structure, which is a six-membered nitrogen-containing heterocycle. This compound features two carbonyl groups at the 2 and 6 positions of the piperidine ring, contributing to its diketone nature. The presence of a hydroxyethyl group and a cyclohexenone moiety enhances its reactivity and potential applications in organic synthesis. The compound is likely to exhibit polar characteristics due to the hydroxyl group, which can engage in hydrogen bonding. Additionally, the presence of multiple functional groups suggests that it may participate in various chemical reactions, including nucleophilic additions and condensation reactions. Its structural complexity indicates potential utility in medicinal chemistry, particularly in the development of pharmaceuticals or agrochemicals. However, specific physical properties such as melting point, boiling point, and solubility would need to be referenced from experimental data for precise applications and handling guidelines.
Formula:C15H21NO4
Synonyms:
  • 2,6-Piperidinedione, 4-[2-(3,5-dimethyl-6-oxo-1-cyclohexen-1-yl)-2-hydroxyethyl]- (9CI)
  • Inactone
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  • Inactone

    CAS:
    <p>Inactone is a biologically active molecule with a 3-pentanoylimino group that inhibits the large ribosomal subunit.</p>
    Formula:C15H21NO4
    Color and Shape:Solid
    Molecular weight:279.332