2-(2-phenyl-1,3-dioxolan-4-yl)piperidine

Identification

Molecular formula

C₁₄H₁₉NO₂

CAS number

80721-64-4

IUPAC name

2-(2-phenyl-1,3-dioxolan-4-yl)piperidine

State

At room temperature, 2-(2-phenyl-1,3-dioxolan-4-yl)piperidine is typically in a solid state. This compound is stable under standard temperature and pressure conditions and is primarily stored as a powder.

Melting point (Celsius)

78.90

Melting point (Kelvin)

352.05

Boiling point (Celsius)

354.40

Boiling point (Kelvin)

627.55

General information

Molecular weight

231.31g/mol

Molar mass

231.3070g/mol

Density

1.1800g/cm³

Appearence

2-(2-phenyl-1,3-dioxolan-4-yl)piperidine typically appears as a white to off-white solid, often in the form of crystalline powder. The color and form can vary slightly depending on the purity and specific conditions of synthesis.

Comment on solubility

Solubility of 2-(2-phenyl-1,3-dioxolan-4-yl)piperidine

The solubility of 2-(2-phenyl-1,3-dioxolan-4-yl)piperidine can be influenced by various factors. Understanding the solubility characteristics of this compound is essential for its applications in different fields such as pharmaceuticals and material sciences. Here are some noteworthy points to consider:

Solvent Interaction: The solubility of this compound may vary significantly depending on the solvent. It is likely to be more soluble in polar solvents due to the presence of functional groups that can engage in hydrogen bonding.
Hydrophobic vs. Hydrophilic: The dioxolane ring can impart some hydrophilic characteristics, while the phenyl group contributes hydrophobic traits. This dual nature can lead to unique solubility profiles in various environments.
Temperature Effects: As with many organic compounds, the solubility can increase with temperature. Experimenting at different temperatures may reveal the optimal conditions for dissolving this compound.

Moreover, it is important to note that empirical data is vital for determining the precise solubility limits. Understanding the solubility behavior of 2-(2-phenyl-1,3-dioxolan-4-yl)piperidine could greatly assist in maximizing its utility in practical applications. As the well-known adage goes, "Like dissolves like," and by taking this into consideration, the appropriate solvent systems can be selected to enhance the solubility of this intriguing compound.

Interesting facts

Fascinating Facts About 2-(2-phenyl-1,3-dioxolan-4-yl)piperidine

2-(2-phenyl-1,3-dioxolan-4-yl)piperidine is a compound that stands out in the realm of organic chemistry due to its intriguing structure and potential applications. Here are some interesting aspects of this compound:

Cyclic Components: The compound features a piperidine ring, which is a six-membered ring containing one nitrogen atom. This heterocyclic structure is common in many pharmaceuticals and contributes to the compound's activity.
Dioxolane Influence: The presence of the 1,3-dioxolane moiety adds unique properties to the compound. Dioxolanes are known to exhibit a range of biological activities, making this compound of particular interest in drug development.
Synthesis Routes: The synthesis of this compound often involves multi-step organic reactions, including the formation of the dioxolane from aldehydes and diols. This complexity can be a great learning experience for students exploring synthetic methods.
Year of Research: Research involving this compound has been increasing since the early 2000s, particularly in the context of its pharmacological properties.
Applications: Compounds like 2-(2-phenyl-1,3-dioxolan-4-yl)piperidine are often explored for their potential as neuroprotective agents, anti-cancer drugs, or in treating central nervous system disorders.

As we delve deeper into the world of organic compounds, 2-(2-phenyl-1,3-dioxolan-4-yl)piperidine serves as a remarkable example of how structure influences function, showcasing the elegance of chemical design and its impact on medicinal chemistry.