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Clorprenaline

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Identification
Molecular formula
C19H20ClNO3
CAS number
4997-55-5
IUPAC name
2-(dimethylamino)ethyl 2-(4-chlorophenoxy)-3-phenyl-prop-2-enoate
State
State
At room temperature, Clorprenaline is a solid. Its stable crystalline form makes it suitable for storage and handling at ambient conditions.
Melting point (Celsius)
75.00
Melting point (Kelvin)
348.15
Boiling point (Celsius)
347.00
Boiling point (Kelvin)
620.15
General information
Molecular weight
349.83g/mol
Molar mass
349.8290g/mol
Density
1.1797g/cm3
Appearence
Clorprenaline appears as a white crystalline powder. Its crystalline nature gives it a shiny, reflective look, and it is typically odorless.
Comment on solubility

Solubility of 2-(dimethylamino)ethyl 2-(4-chlorophenoxy)-3-phenyl-prop-2-enoate

The solubility of 2-(dimethylamino)ethyl 2-(4-chlorophenoxy)-3-phenyl-prop-2-enoate can vary significantly depending on the solvent used and environmental conditions. Understanding solubility is crucial for its applications in pharmaceuticals and other industries. Here are some key points to consider:

  • Polar Solvents: This compound displays limited solubility in polar solvents due to its hydrophobic phenyl groups.
  • Non-Polar Solvents: It is more soluble in non-polar solvents, which can effectively dissolve the phenyl and chlorophenyl moieties.
  • pH Levels: The solubility could change with pH levels due to the presence of the dimethylamino group which can be protonated under acidic conditions.
  • Temperature Influence: Increased temperature generally enhances solubility, making this compound more soluble at elevated temperatures.

In summary, the solubility characteristics of 2-(dimethylamino)ethyl 2-(4-chlorophenoxy)-3-phenyl-prop-2-enoate highlight the importance of solvent selection and environmental factors in its effective use. As with many organic compounds, the interaction with the solvent greatly determines its solubility profile.

Interesting facts

Interesting Facts about 2-(dimethylamino)ethyl 2-(4-chlorophenoxy)-3-phenyl-prop-2-enoate

This compound, known for its complex structure and varied applications, holds a significant place in medicinal chemistry and agricultural applications. Here are some fascinating insights:

  • Diverse Applications: 2-(dimethylamino)ethyl 2-(4-chlorophenoxy)-3-phenyl-prop-2-enoate is primarily explored for its potential as a pharmacological agent. Its structure hints at possible activity in modulating biological systems.
  • Structure-Activity Relationship (SAR): The presence of both a dimethylamino group and a phenyl substituent may influence the compound's interaction with biological targets, possibly increasing potency and selectivity.
  • Environmental Impact: Compounds with chlorinated phenoxy groups often have herbicidal properties, making them valuable in agriculture but raising concerns about their environmental persistence.
  • Synthesis Techniques: The synthesis of this compound can be a fascinating subject of study, employing techniques such as esterification and nucleophilic substitution, which are core concepts in organic chemistry.
  • Research Potential: Ongoing research concerning this compound may lead to the discovery of new therapeutic agents that target specific receptors in the human body.

As noted by one researcher, "The ability of complex esters to exhibit diverse biological activities highlights the intricate relationships between molecular structure and function." This compound exemplifies the profound depth of connections in chemistry, showcasing the importance of structure in determining chemical behavior and applications.


In conclusion, 2-(dimethylamino)ethyl 2-(4-chlorophenoxy)-3-phenyl-prop-2-enoate represents a multidimensional opportunity for exploration in both scientific research and practical applications. Its unique structure not only piques the interest of chemists but also raises important considerations regarding its impact on health and the environment.