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

Identification

Molecular formula

C₁₅H₂₁NO₂

CAS number

65490-91-7

IUPAC name

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

State

At room temperature, 2-(2-benzyl-1,3-dioxolan-4-yl)piperidine is typically in a liquid state, which can be characterized by its viscosity and fluidity under standard conditions.

Melting point (Celsius)

0.00

Melting point (Kelvin)

273.15

Boiling point (Celsius)

306.50

Boiling point (Kelvin)

579.60

General information

Molecular weight

233.31g/mol

Molar mass

233.3120g/mol

Density

1.0700g/cm³

Appearence

2-(2-benzyl-1,3-dioxolan-4-yl)piperidine typically appears as a colorless to pale yellow liquid. Its clarity and consistency can vary depending on its purity and storage conditions.

Comment on solubility

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

The solubility of 2-(2-benzyl-1,3-dioxolan-4-yl)piperidine can be influenced by several factors stemming from its molecular structure and functional groups. Understanding the solubility of this compound is essential for its application in various fields, including pharmaceuticals. Here are some key points to consider:

Polarity: The presence of dioxolane rings introduces a level of polarity to the molecule. This can enhance solubility in polar solvents.
Hydrogen Bonding: The ability of 2-(2-benzyl-1,3-dioxolan-4-yl)piperidine to form hydrogen bonds with solvents can significantly improve its solubility.
Solvent Compatibility: This compound is expected to be soluble in organic solvents such as ethanol and methanol. It may exhibit limited solubility in water due to its hydrophobic benzyl group.
Temperature Effects: Solubility can vary with temperature; thus, higher temperatures might increase solubility in certain solvents.

In general, solubility in organic solvents is greater than that in aqueous solutions, aligning with the common behavior of compounds containing bulky hydrophobic groups.
As a **rule of thumb**, “like dissolves like,” which means that the molecular structure and solvent characteristics must be compatible for optimal solubility.

Interesting facts

Interesting Facts about 2-(2-benzyl-1,3-dioxolan-4-yl)piperidine

This intriguing compound belongs to the class of piperidine derivatives and is notable for its unique structure and potential applications in various fields. Here are some fascinating aspects to consider:

Diverse Applications: Compounds with piperidine rings are often prominent in medicinal chemistry. They are used as scaffolds in the design of pharmacologically active molecules, ranging from anti-inflammatory agents to anti-depressants.
Structural Features: The presence of the 1,3-dioxolan moiety provides distinctive chemical properties. This heterocyclic component can influence the overall reactivity and stability of the compound.
Synthesis Pathways: The synthesis of this compound can involve various methods such as cyclization reactions and nucleophilic substitutions. Understanding the synthetic routes can open avenues for designing even more complex structures.
Biological Interest: The exploration of similar piperidine structures has led to discoveries of compounds that exhibit significant biological activity, showcasing the promise of this class in drug design.
Research Advancements: As research continues to evolve, compounds like 2-(2-benzyl-1,3-dioxolan-4-yl)piperidine offer the possibility of discovering novel therapeutic agents, particularly in combating diseases where current treatments are inadequate.

Overall, 2-(2-benzyl-1,3-dioxolan-4-yl)piperidine exemplifies the exciting nature of chemical compounds in the realm of organic chemistry, illustrating how simple modifications can lead to profound implications in science and medicine.