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Ethylphenylimidazolidinone

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Identification
Molecular formula
C11H15N2O
CAS number
67032-98-8
IUPAC name
1-ethyl-3-phenyl-imidazolidin-2-one
State
State

Under standard conditions (at room temperature), 1-Ethyl-3-phenyl-imidazolidin-2-one is typically found as a liquid. It becomes a solid upon cooling to its melting point.

Melting point (Celsius)
46.00
Melting point (Kelvin)
319.15
Boiling point (Celsius)
315.00
Boiling point (Kelvin)
588.15
General information
Molecular weight
190.25g/mol
Molar mass
190.2460g/mol
Density
1.1780g/cm3
Appearence

1-Ethyl-3-phenyl-imidazolidin-2-one is a colorless to pale-yellow liquid. It is known for its characteristic odor. In its pure form, the compound tends to present itself as a clear and stable liquid under standard conditions.

Comment on solubility

Solubility of 1-ethyl-3-phenyl-imidazolidin-2-one

The solubility of 1-ethyl-3-phenyl-imidazolidin-2-one in various solvents can be summarized as follows:

  • Polar solvents: This compound exhibits reasonable solubility in polar solvents such as water and methanol. The presence of the amino group often contributes to hydrogen bonding, enhancing its solubility in these environments.
  • Non-polar solvents: Conversely, when dissolved in non-polar solvents like hexane or toluene, the solubility is generally low. The aromatic phenyl group, while capable of some degree of interaction, does not compensate enough for the less polar nature of these solvents.
  • Temperature effects: Increased temperature can lead to improved solubility across the board. As the temperature rises, kinetic energy increases, often allowing molecules to overcome solvation barriers more effectively.
  • Concentration effects: At higher concentrations, precipitation can occur in both polar and non-polar environments, indicating a limit to its solubility.

In conclusion, while 1-ethyl-3-phenyl-imidazolidin-2-one shows versatile solubility characteristics, the choice of solvent significantly impacts its solubility profile. These factors are crucial for applications in pharmaceuticals and materials science, where the solubility of compounds can dictate their effectiveness and utility.

Interesting facts

Interesting Facts about 1-Ethyl-3-phenyl-imidazolidin-2-one

1-Ethyl-3-phenyl-imidazolidin-2-one is an intriguing compound in the realm of organic chemistry, particularly due to its unique structure and potential applications. Here are some engaging insights:

  • Structural Significance: The compound features a five-membered ring, which incorporates both nitrogen and carbon atoms. This imidazolidinone structure is an essential framework in medicinal chemistry.
  • Biological Relevance: Compounds containing imidazolidinone moieties have attracted attention for their biological activities, including anti-inflammatory and antitumor properties. This raises the possibility that 1-ethyl-3-phenyl-imidazolidin-2-one could be explored for similar applications in drug development.
  • Versatile Reactivity: The nitrogen atoms in the ring can participate in various chemical reactions, making it valuable in synthetic organic chemistry. The compound can act as a nucleophile or participate in cyclization processes, furthering its role in the synthesis of other complex molecules.
  • Chirality and Isomerism: Depending on the substitution on the phenyl and ethyl groups, 1-ethyl-3-phenyl-imidazolidin-2-one can exhibit chirality, leading to various isomers. Understanding the properties of these isomers can provide insights into how they might behave in biological systems.
  • Research Potential: Given its unique properties and structural attributes, this compound presents exciting opportunities for research in material science and pharmacology, promoting ongoing studies to uncover new functionalities.

As a reminder, the exploration of compounds like 1-ethyl-3-phenyl-imidazolidin-2-one is not just about understanding their structure but also about investigating their potential impacts on technology and health.

Synonyms
SCHEMBL8393737