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Diethylcarbophenoxy chloride

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Identification
Molecular formula
C13H18Cl2N2O2
CAS number
82-15-1
IUPAC name
2-(diethylamino)ethyl N-(2,5-dichlorophenyl)carbamate
State
State

At room temperature, it is typically found in a solid state.

Melting point (Celsius)
46.00
Melting point (Kelvin)
319.15
Boiling point (Celsius)
360.30
Boiling point (Kelvin)
633.50
General information
Molecular weight
290.19g/mol
Molar mass
290.1850g/mol
Density
1.2100g/cm3
Appearence

It appears as a white to off-white crystalline solid.

Comment on solubility

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

The solubility of 2-(diethylamino)ethyl N-(2,5-dichlorophenyl)carbamate is influenced by several factors, including its molecular structure and functional groups. Understanding these factors can help predict how this compound behaves in various solvents.

Factors Affecting Solubility:

  • Polarity: The presence of a carbamate group often increases polarity, potentially enhancing solubility in polar solvents like water.
  • Hydrophobic Interactions: The diethylamino group adds hydrophobic character, which may limit solubility in highly polar environments.
  • Chlorine Atoms: The presence of two chlorine atoms on the aromatic ring can further influence solubility due to their electronegative nature, affecting intermolecular interactions.

As a result, the solubility of this compound can vary significantly depending on its environment. Common trends in solubility include:

  • This compound may exhibit increased solubility in organic solvents such as alcohols or acetone.
  • It may have limited solubility in aqueous solutions due to its hydrophobic characteristics.
  • Temperature can also play a role; typically, solubility increases with rising temperature.

In conclusion, while 2-(diethylamino)ethyl N-(2,5-dichlorophenyl)carbamate demonstrates some degree of solubility in various solvents, its behavior is highly dependent on the specific conditions. Understanding these solubility characteristics is crucial for applications in chemical processes and product formulation.

Interesting facts

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

2-(Diethylamino)ethyl N-(2,5-dichlorophenyl)carbamate is a unique compound that has drawn interest in the field of chemistry and pharmacology for several reasons:

  • Pesticide Use: This compound is primarily known for its application as a pesticide. Its structure allows it to effectively target pests while minimizing harm to beneficial organisms, making it a valuable tool in agricultural practices.
  • Chemical Structure: The presence of the 2,5-dichlorophenyl group is significant because the chlorine atoms enhance the compound's overall biological activity. Chlorinated aromatic compounds like this one exhibit a range of interactions with biological systems, making them of interest for further study.
  • Versatile Activity: Beyond its use as a pesticide, the compounds of this class may have potential pharmaceutical applications. The diethylamino group is well-regarded for its ability to influence the pharmacokinetics of drugs, potentially leading to innovative therapeutic options.
  • Toxicology and Safety: Given its chemical nature, it is crucial to study the toxicological profile of this compound. Understanding its environmental impact and safe usage levels is essential in both agriculture and potential therapeutic applications.

As with many chemical compounds, 2-(diethylamino)ethyl N-(2,5-dichlorophenyl)carbamate illustrates the intricate balance between utility and safety, inviting more in-depth research and discussion in scientific circles.

Further investigations can yield insights not only into its practical applications but also into the broader implications of using such chemical structures in our environments.