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2-(1-piperidylimino)-1-(p-tolyl)ethanone

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Identification
Molecular formula
C14H18N2O
CAS number
67065-38-7
IUPAC name
2-(1-piperidylimino)-1-(p-tolyl)ethanone
State
State

This compound is commonly a solid at room temperature.

Melting point (Celsius)
205.70
Melting point (Kelvin)
478.90
Boiling point (Celsius)
345.30
Boiling point (Kelvin)
618.50
General information
Molecular weight
230.31g/mol
Molar mass
230.3290g/mol
Density
1.0700g/cm3
Appearence

The compound typically appears as a crystalline solid. The exact color and form can vary but is generally an off-white to pale yellowish solid. It might also exist in powdered form depending on the method of preparation.

Comment on solubility

Solubility of 2-(1-piperidylimino)-1-(p-tolyl)ethanone

The solubility of 2-(1-piperidylimino)-1-(p-tolyl)ethanone can be influenced by several factors, primarily its molecular structure and functional groups. This compound, characterized by a piperidine ring and an aromatic p-tolyl group, suggests that it may have varying solubility in different solvents.

Factors Affecting Solubility:

  • Molecular Size: Larger molecules typically exhibit lower solubility due to decreased interactions with solvent molecules.
  • Polarity: The presence of polar functional groups can enhance solubility in polar solvents but reduce it in non-polar solvents.
  • Hydrogen Bonding: The ability to form hydrogen bonds can significantly increase solubility in water.

In general, 2-(1-piperidylimino)-1-(p-tolyl)ethanone may display good solubility in polar organic solvents such as ethanol or dimethyl sulfoxide (DMSO), as opposed to non-polar solvents like hexane. An interesting takeaway is that “like dissolves like,” which implies that the solvent properties must match the molecular characteristics of the compound.

Overall, while the precise solubility can vary, understanding these underlying principles provides valuable insights for predicting behavior in different environments.

Interesting facts

Interesting Facts about 2-(1-piperidylimino)-1-(p-tolyl)ethanone

This compound, known for its unique structural features, showcases a fascinating blend of organic chemistry and medicinal application.

  • Functional Group Diversity: The presence of a piperidyl group and an ethanone moiety introduces various functional characteristics, making it a versatile building block in organic synthesis.
  • Pharmacological Potential: Compounds containing a piperidyl nitrogen have been widely studied for their potential biological activity. This particular compound may hold promise in the development of new pharmaceuticals, particularly as it may interact with biological targets in the central nervous system.
  • Synthetic Utility: The synthesis of 2-(1-piperidylimino)-1-(p-tolyl)ethanone often involves multiple methodologies, showcasing its relevance in synthetic organic chemistry. Chemists appreciate how modifying the p-tolyl group can lead to various derivatives with altered properties.
  • Research Application: It serves as a model compound in studying the reactivity and mechanism of piperidine-based derivatives, helping researchers understand larger molecular frameworks.
  • 2D and 3D Structural Considerations: Understanding the spatial arrangement of this compound via techniques such as NMR and X-ray crystallography can provide insights into its reactivity and interaction with other molecules.

In summary, 2-(1-piperidylimino)-1-(p-tolyl)ethanone is not just another intricate molecular design; it represents the intersection of chemistry, pharmacology, and innovation, potentially paving the way for new discoveries in medicinal chemistry.