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not commonly named

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Identification
Molecular formula
C19H21N2O
CAS number
143365-46-6
IUPAC name
1-(4-phenylphenyl)-2-(1-piperidylimino)ethanone
State
State
At room temperature, it is typically a solid compound, indicating a stable crystalline structure.
Melting point (Celsius)
105.00
Melting point (Kelvin)
378.15
Boiling point (Celsius)
475.00
Boiling point (Kelvin)
748.15
General information
Molecular weight
276.37g/mol
Molar mass
276.3710g/mol
Density
1.1600g/cm3
Appearence

The compound generally appears as a crystalline solid. The specific color may vary depending on the level of purity, from white to off-white.

Comment on solubility

Solubility of 1-(4-phenylphenyl)-2-(1-piperidylimino)ethanone

Understanding the solubility of 1-(4-phenylphenyl)-2-(1-piperidylimino)ethanone is crucial for its application in various chemical processes. The solubility of this compound can be influenced by several factors:

  • Polarity: The presence of both aromatic and amine functional groups suggests a mixed polarity that may affect solubility in different solvents.
  • Solvent Interaction: This compound is likely to be more soluble in polar organic solvents, such as ethanol and methanol, due to potential dipole-dipole interactions.
  • Temperature Impact: As with many organic compounds, an increase in temperature generally enhances solubility by providing more kinetic energy to break intermolecular interactions.

It is important to note that while specific solubility data might not be readily available, one can evaluate solubility through empirical methods and by examining the structural characteristics of the compound. Further studies may be necessary to explore its solubility profile in various environments.

Interesting facts

Interesting Facts about 1-(4-phenylphenyl)-2-(1-piperidylimino)ethanone

1-(4-phenylphenyl)-2-(1-piperidylimino)ethanone is a fascinating compound of significant interest in the field of organic chemistry. This compound features both aromatic and aliphatic elements, making it a valuable subject for various studies, particularly in medicinal chemistry and materials science.

Key Features

  • Structural Diversity: The compound showcases a unique structure that combines a piperidine ring with a ketone group, facilitating potential applications in drug design.
  • Biological Activity: Compounds similar to this one have been shown to exhibit various biological activities, making them candidates for therapeutic applications.
  • Research Potential: Its intriguing formulation opens the door to research in photochemistry and photophysics, wherein the interaction of light with molecules can lead to exciting findings.
  • Synthetic Applications: The methodology for synthesizing this compound often involves innovative reactions that can lead to the development of new synthetic pathways in organic chemistry.

As a chemical scientist, one might be particularly intrigued by the compound’s potential use in the field of material science. The presence of both piperidine and phenyl functionalities allows for a rich canvas for modifications, which could enhance the compound's properties for applications in developing new materials or drugs.

In summary, the study of 1-(4-phenylphenyl)-2-(1-piperidylimino)ethanone not only bridges various subfields within chemistry but also illuminates the multifaceted nature of organic compounds in addressing contemporary challenges in science and technology. As noted by chemists, “The beauty of organic chemistry lies in the infinite variations and functional potentials of its compounds.”