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Carbamoyl-2,5-dichloroaniline

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Identification
Molecular formula
C14H18Cl2N2O2
CAS number
77146-51-3
IUPAC name
2-(1-piperidyl)ethyl N-(2,5-dichlorophenyl)carbamate
State
State
The compound is a solid at room temperature. It is stable under standard conditions, but should be kept away from excessive moisture and heat to prevent any chemical degradation.
Melting point (Celsius)
135.00
Melting point (Kelvin)
408.15
Boiling point (Celsius)
407.20
Boiling point (Kelvin)
680.35
General information
Molecular weight
333.21g/mol
Molar mass
333.1900g/mol
Density
1.3900g/cm3
Appearence

The compound is typically found as a solid crystalline powder. It may appear white to off-white in color, depending on its purity and form.

Comment on solubility

Solubility of 2-(1-piperidyl)ethyl N-(2,5-dichlorophenyl)carbamate

The solubility of 2-(1-piperidyl)ethyl N-(2,5-dichlorophenyl)carbamate can be influenced by several factors, making it an interesting subject for discussion. Generally, the solubility of a compound in a particular solvent depends on its chemical structure and polar/non-polar characteristics.

Key Factors Influencing Solubility:

  • Polarity: The presence of both polar functional groups, such as the carbamate moiety, and relatively non-polar aromatic rings can lead to varied solubility in polar versus non-polar solvents.
  • Hydrogen Bonding: This compound may engage in hydrogen bonding due to the hydroxyl and amine groups, enhancing its solubility in polar solvents like water.
  • Temperature: Increased temperature generally enhances solubility for many organic compounds; thus, warming a solution may facilitate the dissolving process for this carbamate.

In conclusion, while the solubility behavior of 2-(1-piperidyl)ethyl N-(2,5-dichlorophenyl)carbamate can vary significantly based on the solvent used and environmental conditions, it commonly finds better solubility in polar organic solvents rather than non-polar counterparts. As with many chemical compounds, the specific solubility attributes would ideally be confirmed through empirical testing.

Interesting facts

Interesting Facts about 2-(1-piperidyl)ethyl N-(2,5-dichlorophenyl)carbamate

2-(1-piperidyl)ethyl N-(2,5-dichlorophenyl)carbamate, commonly recognized in the realm of pharmaceuticals and chemistry, showcases a fascinating combination of chemical properties and biological potential. Here are some engaging insights about this compound:

  • Pharmaceutical Applications: This compound has garnered attention for its potential use in therapeutic applications, particularly in the field of neurology and psychiatry. Its structural composition is thought to interact with neurotransmitter systems in the brain.
  • Mechanism of Action: The inclusion of the piperidine moiety suggests intriguing interactions with receptor sites, potentially influencing mood and cognition. Such mechanisms could pave the way for developing treatments for various neurological disorders.
  • Synthetic Pathways: Chemists have developed several methods for synthesizing this compound, each providing unique challenges and learning opportunities. Understanding these synthesis routes can enhance students' grasp of organic chemistry techniques.
  • Structure-Activity Relationship: Studying how modifications in the structure of 2-(1-piperidyl)ethyl N-(2,5-dichlorophenyl)carbamate impact its biological activity allows scientists to design more effective derivatives with improved efficacy and reduced side effects.
  • Environmental Impact: As with many chemical compounds, it's vital to consider the environmental implications of its synthesis and use. Researchers are increasingly focused on developing greener synthesis techniques to minimize adverse effects.

This compound is not just a collection of atoms; it represents a wealth of knowledge and potential waiting to be explored in the realm of chemical science. As we delve deeper into its properties and applications, the journey into understanding this compound reveals the intricacies of chemical interactions and innovations in medicine.