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Meclofenoxate

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Identification
Molecular formula
C14H18ClNO2
CAS number
51-68-3
IUPAC name
2-(1-piperidyl)ethyl N-(3-chloro-2-methyl-phenyl)carbamate
State
State

At room temperature, Meclofenoxate is in a solid crystalline form. It is typically stable under normal conditions of use and storage.

Melting point (Celsius)
123.00
Melting point (Kelvin)
396.15
Boiling point (Celsius)
418.50
Boiling point (Kelvin)
691.65
General information
Molecular weight
267.75g/mol
Molar mass
267.7520g/mol
Density
1.1300g/cm3
Appearence

Meclofenoxate is typically found as a white to off-white crystalline powder. It may sometimes appear slightly yellowish upon prolonged exposure to air or light.

Comment on solubility

Solubility of 2-(1-piperidyl)ethyl N-(3-chloro-2-methyl-phenyl)carbamate

The solubility of 2-(1-piperidyl)ethyl N-(3-chloro-2-methyl-phenyl)carbamate can be characterized by several factors that influence its behavior in various solvents. This compound is a carbamate derivative which typically suggests a certain level of polarity, influencing its interactions with solvents.

When considering its solubility, some key points include:

  • Polarity: The presence of the piperidyl group contributes to the overall polarity of the molecule, which can enhance solubility in polar solvents such as water and alcohols.
  • Functional Groups: The carbamate functional group (-NH-CO-O-) is known to form hydrogen bonds, potentially increasing solubility in aqueous environments.
  • Hydrophobic Interactions: The aromatic ring from the 3-chloro-2-methyl-phenyl part may create hydrophobic interactions that could reduce solubility in very polar solvents but improve compatibility with organic solvents.

It is essential to consider that experimental solubility can vary, and the interactions with solvents depend heavily on the specific conditions, such as temperature and pH. In summary, the solubility of 2-(1-piperidyl)ethyl N-(3-chloro-2-methyl-phenyl)carbamate is influenced by a combination of its polar and non-polar characteristics, which could lead to interesting solubility profiles in different solvent systems.

Interesting facts

Interesting Facts About 2-(1-Piperidyl)ethyl N-(3-chloro-2-methyl-phenyl)carbamate

This compound is a fascinating example of a carbamate, which plays a crucial role in medicinal chemistry. Carbamates are derivatives of carbamic acid and are known for their various applications in pharmaceuticals. Here are some intriguing aspects of this particular compound:

  • Structural Complexity: The presence of a piperidine ring contributes to the compound's structural intricacy, which can influence its biological activity.
  • Biological Relevance: Compounds featuring piperidine moieties are often associated with neurotransmitter regulation and have been studied for their potential as antidepressants and anxiolytics.
  • Antimicrobial Activity: The chlorinated phenyl group suggests that this compound might exhibit antimicrobial properties, making it an interesting candidate for further research in drug development.
  • Mechanism of Action: Understanding how this molecule interacts at the molecular level can reveal insights into drug design and efficacy, particularly in targeting specific receptors.
  • Variability in Function: The modifications on the aromatic ring can significantly alter the compound’s pharmacokinetics and pharmacodynamics, affecting how it is processed by the body.

In the words of a famous chemist, "Innovation is the ability to see change as an opportunity - not a threat.” This compound showcases the innovative nature of chemistry as scientists explore new avenues for drug development and therapeutic interventions.

Overall, 2-(1-piperidyl)ethyl N-(3-chloro-2-methyl-phenyl)carbamate not only exemplifies the complex beauty of organic chemistry but also stands as a potential beacon for future medical advancements.