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Cinnamyl diethylamine ester

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Identification
Molecular formula
C15H21NO2
CAS number
102-09-0
IUPAC name
3-(diethylamino)propyl 3-phenylprop-2-enoate
State
State

The compound is typically in a liquid state at room temperature, owing to its relatively low melting point of around -45°C.

Melting point (Celsius)
-45.00
Melting point (Kelvin)
228.15
Boiling point (Celsius)
321.20
Boiling point (Kelvin)
594.35
General information
Molecular weight
219.31g/mol
Molar mass
219.3120g/mol
Density
1.0075g/cm3
Appearence

This compound appears as a colorless to pale yellow liquid. Due to its chemical structure, it may exhibit a faint aromatic odor. Exposure to air may cause it to darken in color.

Comment on solubility

Solubility of 3-(diethylamino)propyl 3-phenylprop-2-enoate

The solubility of 3-(diethylamino)propyl 3-phenylprop-2-enoate in various solvents plays a critical role in its application across different fields. This compound, characterized by its unique structure, exhibits variable solubility which can be influenced by several factors:

  • Polarity of the solvent: As a result of its polar diethylamino group, this compound is likely to demonstrate good solubility in polar organic solvents, such as:
    • Dimethyl sulfoxide (DMSO)
    • Acetone
    • Alcohols (e.g., ethanol, methanol)
  • Non-polar solvents: Conversely, solubility in non-polar solvents may be limited due to the presence of the polar functional groups.
  • Temperature effects: Generally, an increase in temperature can enhance solubility, allowing for better interaction between the compound and solvent molecules.

In practical applications, knowing that “solubility is key to effective formulation and reactivity” can help researchers optimize conditions for synthesis and usage. Special attention should be given to the specific solvent environment to achieve desired outcomes, emphasizing the need for comprehensive solubility profiling to unlock the full potential of 3-(diethylamino)propyl 3-phenylprop-2-enoate.

Interesting facts

Interesting Facts about 3-(Diethylamino)propyl 3-phenylprop-2-enoate

3-(Diethylamino)propyl 3-phenylprop-2-enoate is a fascinating compound that beckons attention due to its unique structural properties and diverse applications in the field of chemistry. This compound can be highlighted through several notable aspects:

  • Biological Activity: This compound has garnered interest in the pharmaceutical industry due to its potential biological activity. Its unique structure allows it to interact with various biological pathways, making it a candidate for drug development.
  • Versatile Functional Groups: The presence of diethylamino and phenyl substituents enriches its chemical reactivity. These groups can facilitate a variety of chemical reactions, enabling the synthesis of derivatives that may exhibit enhanced properties.
  • Synthetic Pathways: The synthesis of 3-(diethylamino)propyl 3-phenylprop-2-enoate involves innovative organic reactions, showcasing the art of synthesis within organic chemistry. Students and chemists can explore multiple synthetic routes, learning about the intricacies of reaction mechanisms.
  • Industrial Applications: Due to its unique characteristics, this compound may find applications in the formulation of agrochemicals, additives, or functional materials, playing a crucial role in enhancing product performance in various industries.

Moreover, the study of such compounds not only enriches our understanding of organic chemistry but also challenges students to think critically about molecular interactions and applications in real-world scenarios. As the scientific community continues to explore its potential, 3-(diethylamino)propyl 3-phenylprop-2-enoate stands as a testament to the power of organic compounds in medicinal chemistry and material science.

Synonyms
3-(Diethylamino)propylcinnamate
DB-338966
benzene, 2-[3-(diethylamino)propoxycarbonyl]vinyl-