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Piperalin

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Identification
Molecular formula
C19H22N2O3
CAS number
3478-94-2
IUPAC name
2-(1-piperidyl)ethyl N-(2-phenoxyphenyl)carbamate
State
State

At room temperature, Piperalin is typically a crystalline solid.

Melting point (Celsius)
44.00
Melting point (Kelvin)
317.15
Boiling point (Celsius)
277.00
Boiling point (Kelvin)
550.15
General information
Molecular weight
327.39g/mol
Molar mass
327.3900g/mol
Density
1.1720g/cm3
Appearence

Piperalin typically appears as a colorless to pale yellow liquid. It does not have any distinct odor.

Comment on solubility

Solubility of 2-(1-piperidyl)ethyl N-(2-phenoxyphenyl)carbamate

The solubility of 2-(1-piperidyl)ethyl N-(2-phenoxyphenyl)carbamate presents some intriguing characteristics that are worth noting. This compound has unique structural features that can influence its interactions with solvents. Here are some key points regarding its solubility:

  • Polarity: The presence of both the piperidine moiety and the phenoxyphenyl group suggests moderate polarity. This can lead to solubility in both polar and non-polar solvents, although optimal conditions will vary.
  • Hydrogen Bonding: The functional groups within the molecule may facilitate hydrogen bonding, enhancing solubility in polar solvents such as water or alcohols.
  • Cation-π Interactions: The aromatic system might engage in cation-π interactions with other components in solution, which can further influence solubility.
  • Temperature Dependency: As with many organic compounds, increased temperature can lead to increased solubility, allowing for better dissolution in various media.

In summary, while 2-(1-piperidyl)ethyl N-(2-phenoxyphenyl)carbamate may demonstrate a certain degree of solubility in suitable solvents, understanding the specific conditions under which this solubility occurs is crucial for applications in both synthetic and industrial chemistry. Experimentation under varying conditions will provide a clearer picture of its solubility profile.

Interesting facts

Interesting Facts about 2-(1-Piperidyl)ethyl N-(2-phenoxyphenyl)carbamate

The compound 2-(1-piperidyl)ethyl N-(2-phenoxyphenyl)carbamate is a fascinating member of the carbamate family, showcasing a blend of properties that make it an interesting subject of study in medicinal chemistry. Here are some notable aspects:

  • Structural Complexity: This compound contains a piperidine ring, which is notable for its presence in various biologically active molecules. The structure enhances its potential interactions within biological systems.
  • Biological Activity: Derivatives of carbamates often exhibit a wide range of pharmacological activities, including antimicrobial and antidepressant effects. Research into this compound may reveal potential therapeutic applications.
  • Synthesis Insights: The synthesis of carbamates often involves straightforward methodologies that are valuable for students learning organic chemistry. This compound can be prepared using easily accessible starting materials, providing a practical example for laboratory study.
  • Intermolecular Interactions: The unique substituent patterns in 2-(1-piperidyl)ethyl N-(2-phenoxyphenyl)carbamate may contribute to its ability to form hydrogen bonds and π-π interactions, which are essential for understanding its reactivity and physical properties.
  • Potential Research Applications: The combination of the piperidine moiety with a phenoxyphenyl group indicates that there is potential for further exploration in the field of drug design, specifically in developing new pharmaceuticals that can target difficult diseases.

As a compound that bridges the gap between organic synthesis and biological relevance, 2-(1-piperidyl)ethyl N-(2-phenoxyphenyl)carbamate is a prime example of how chemical compounds can offer insights into both the chemical and biological sciences.