Skip to main content

Heptaminol

ADVERTISEMENT
Identification
Molecular formula
C15H23ClN2O2
CAS number
5571-36-8
IUPAC name
2-(1-piperidyl)ethyl N-(5-chloro-2-methyl-phenyl)carbamate
State
State

At room temperature, heptaminol exists as a solid and is usually encountered as a white crystalline powder. It is stable under normal conditions, making it suitable for handling and storage as a solid compound.

Melting point (Celsius)
174.00
Melting point (Kelvin)
447.15
Boiling point (Celsius)
397.00
Boiling point (Kelvin)
670.15
General information
Molecular weight
313.81g/mol
Molar mass
313.8060g/mol
Density
1.2000g/cm3
Appearence

Heptaminol typically appears as a white, crystalline powder. It is often supplied in this physical form when used in pharmaceutical formulations or research settings. The powder is generally free-flowing, meaning it does not clump together easily.

Comment on solubility

Solubility of 2-(1-piperidyl)ethyl N-(5-chloro-2-methyl-phenyl)carbamate

The solubility of 2-(1-piperidyl)ethyl N-(5-chloro-2-methyl-phenyl)carbamate can be influenced by various factors, given its complex molecular structure. Generally, the presence of a piperidyl group often indicates potential for moderate to good solubility in polar solvents due to its nitrogen-containing structure,
which allows for favorable interactions such as hydrogen bonding.

Factors Influencing Solubility:

  • Polarity of the solvent: This compound is likely to dissolve more readily in polar solvents like methanol or ethanol compared to non-polar solvents.
  • Temperature: Increasing temperature typically enhances solubility for many organic compounds, enhancing the kinetic energy of molecules.
  • Concentration of solute: At higher concentrations, one might observe reduced solubility due to saturation effects.
  • pH level: Since carbamate groups can be sensitive to pH, adjustments in acidity could affect solubility.

As a general guideline, while the specific solubility of this compound may not be readily available, exploring solubility in various solvent systems can provide insight into its practical applications. The likelihood of favorable solubility underscores its potential utility in various formulations and reactions.

Interesting facts

Interesting Facts about 2-(1-Piperidyl)ethyl N-(5-chloro-2-methyl-phenyl)carbamate

2-(1-Piperidyl)ethyl N-(5-chloro-2-methyl-phenyl)carbamate is an intriguing compound that belongs to the category of carbamates, which are esters of carbonic acid. This specific compound presents a fascinating blend of functional groups and structural characteristics that make it a subject of interest in medicinal chemistry.

Key Features:

  • Biological Activity: Carbamates often exhibit a variety of biological activities, with some derivatives showcasing potential as pharmaceuticals. Their ability to act as enzyme inhibitors or neurotransmitter modulators makes them essential in drug development.
  • Structural Complexity: The presence of the piperidine ring along with the chloro and methyl substituents creates a complex three-dimensional shape, allowing for diverse interaction patterns with biological targets.
  • Applications: Compounds like this one are explored for their potential therapeutic applications, particularly in the fields of psychiatry and neurology.

Historical Context:

This compound is notable not just for its structural features, but also for its historical context. The exploration of carbamate derivatives has led to significant pharmacological discoveries. As the renowned chemist Yoshito Kishi once stated, “The complexity of nature provides endless inspiration for synthesis.” This perfectly encapsulates the essence of studying compounds like 2-(1-piperidyl)ethyl N-(5-chloro-2-methyl-phenyl)carbamate.

Research and Development:

Ongoing research in this area includes:

  • Investigating the compound's efficacy as an antiparasitic agent.
  • Studying its potential neuroprotective effects.
  • Exploring its pharmacokinetics and bioavailability to optimize therapeutic applications.

In conclusion, 2-(1-Piperidyl)ethyl N-(5-chloro-2-methyl-phenyl)carbamate exemplifies the rich tapestry of organic chemistry, where intricate molecular designs lead to valuable insights in the realm of medicinal chemistry. Its unique properties and implications for future research highlight the importance of syntax in chemical synthesis and the continuous quest for innovation in the pharmaceutical industry.