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Naphthylpyrovalerone

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Identification
Molecular formula
C22H29N1
CAS number
850352-53-3
IUPAC name
2-(1-naphthyl)-N-[2-(1-piperidyl)ethyl]hex-4-en-1-amine
State
State
Naphthylpyrovalerone is typically found as a solid at room temperature, often in the form of a crystalline powder.
Melting point (Celsius)
75.00
Melting point (Kelvin)
348.00
Boiling point (Celsius)
274.00
Boiling point (Kelvin)
547.00
General information
Molecular weight
327.49g/mol
Molar mass
327.4960g/mol
Density
1.1500g/cm3
Appearence

Naphthylpyrovalerone is a crystalline solid. It can appear as white or off-white crystals, depending on the purity and method of preparation.

Comment on solubility

Solubility of 2-(1-naphthyl)-N-[2-(1-piperidyl)ethyl]hex-4-en-1-amine

When assessing the solubility of the compound 2-(1-naphthyl)-N-[2-(1-piperidyl)ethyl]hex-4-en-1-amine (C22H29N1), several important factors come into play:

  • Polarity: The compound exhibits moderate polarity due to the presence of both aromatic and aliphatic sections, which can influence its solubility in different solvents.
  • Solvent Interaction: This compound may show good solubility in organic solvents, such as ethanol or acetone, owing to its hydrophobic naphthyl group, while being less soluble in water.
  • Temperature Dependence: As is common with many organic compounds, solubility can increase with temperature.

In summary, the solubility characteristics of this compound demonstrate the interaction between its functional groups and the solvent environment. It serves as a reminder of the intricate balance between structure and solubility in organic chemistry, where "like dissolves like" plays a crucial role.

Interesting facts

Interesting Facts about 2-(1-naphthyl)-N-[2-(1-piperidyl)ethyl]hex-4-en-1-amine

This compound, known as 2-(1-naphthyl)-N-[2-(1-piperidyl)ethyl]hex-4-en-1-amine, boasts a fascinating structure and an array of potential applications in the field of medicinal chemistry.

Structural Significance

  • Naphthalene Ring: The presence of the 1-naphthyl group contributes significantly to its aromatic characteristics, which can influence its biological activity.
  • Piperidine Moiety: The 1-piperidyl segment offers properties that can enhance receptor binding, making it interesting for pharmacological studies.
  • Double Bond: The hex-4-en-1-amino configuration introduces cis and trans geometric isomerism, yielding compounds with distinct properties and activities.

Potential Applications

This compound could be of particular interest to scientists and researchers focused on:

  • Drug Development: With unique structural features, it might be explored as a precursor in creating novel pharmaceuticals.
  • Neuroscience: Its ability to interact with various neurotransmitter receptors positions it as a potential candidate for studies related to cognitive functions.
  • Aromatic Compounds: The aromatic functionality can lead to interesting insights into its interactions with other chemical systems.

Important Insights

It is important to note that the study of such compounds is crucial for advancing our understanding of complex biochemical interactions. As one researcher noted, "The marriage of amine properties with aromatic frameworks is where chemistry reveals its most enchanting attributes."

As research continues, 2-(1-naphthyl)-N-[2-(1-piperidyl)ethyl]hex-4-en-1-amine may unveil further mysteries, potentially unlocking new pathways for therapeutic interventions.