Skip to main content

Ethyl 2,5-dioxo-4,4-diphenylimidazolidine-1-carboxylate

ADVERTISEMENT
Identification
Molecular formula
C18H16N2O4
CAS number
6325-25-5
IUPAC name
ethyl 2,5-dioxo-4,4-diphenyl-imidazolidine-1-carboxylate
State
State

This compound is typically a solid at room temperature.

Melting point (Celsius)
160.00
Melting point (Kelvin)
433.15
Boiling point (Celsius)
372.00
Boiling point (Kelvin)
645.15
General information
Molecular weight
332.35g/mol
Molar mass
332.3530g/mol
Density
1.2700g/cm3
Appearence

Appearance: This compound typically appears as a white to off-white crystalline powder.

Comment on solubility

Solubility of Ethyl 2,5-Dioxo-4,4-Diphenyl-Imidazolidine-1-Carboxylate

When examining the solubility of ethyl 2,5-dioxo-4,4-diphenyl-imidazolidine-1-carboxylate, it is essential to consider the underlying structural features that influence its behavior in different solvents.

Key factors affecting solubility include:

  • Polarity: The presence of polar and nonpolar groups in the structure typically determines how well the compound will dissolve in polar solvents (like water) versus nonpolar solvents (like hexane).
  • Hydrogen bonding: The ability of the molecule to engage in hydrogen bonding can enhance solubility in polar solvents.
  • Molecular weight: Higher molecular weight compounds may exhibit reduced solubility due to steric hindrance and larger molecular size.

It is often said, "Like dissolves like." Therefore, you can expect that ethyl 2,5-dioxo-4,4-diphenyl-imidazolidine-1-carboxylate will be more soluble in nonpolar organic solvents rather than in water. However, the specific solubility characteristics can only be definitively determined through empirical experimentation.

Interesting facts

Interesting Facts about Ethyl 2,5-Dioxo-4,4-Diphenyl-Imidazolidine-1-Carboxylate

Ethyl 2,5-dioxo-4,4-diphenyl-imidazolidine-1-carboxylate is a fascinating compound in the realm of organic chemistry, notable for its structural complexity and potential applications. Here are some interesting insights about this intriguing molecule:

  • Diverse Applications: Compounds of this nature are often examined for their utility in medicinal chemistry, especially in the development of pharmaceuticals. Their unique structure can impart specific biological activities, making them candidates for drug discovery.
  • Imidazolidine Core: The presence of the imidazolidine ring, which features both nitrogen and carbon atoms in its structure, is quite significant. This ring system is often associated with various biological activities, including anti-inflammatory and anti-cancer properties.
  • Synthetic Pathways: The synthesis of this compound can involve various organic reactions, including condensation and acylation processes. Understanding the synthetic pathways can provide valuable insights into reaction mechanisms and the reactivity of different functional groups.
  • Pharmaceutical Insights: Ethyl esters are known to enhance the bioavailability of compounds, potentially leading to increased effectiveness in therapeutic applications. The ethyl group in this compound may play a crucial role in its pharmacokinetic profile.
  • Research Significance: Studies involving this compound may yield important findings in the fields of materials science and organic electronics. Its unique properties could be harnessed for developing novel materials with specific functionalities.

In summary, ethyl 2,5-dioxo-4,4-diphenyl-imidazolidine-1-carboxylate is not just an ordinary compound; it combines a rich chemical structure with a breadth of potential applications spanning from medicine to materials science. As we continue to explore its properties and interactions, we unveil new opportunities for innovation in various scientific fields.

Synonyms
1097-57-0
1-IMIDAZOLIDINECARBOXYLIC ACID, 2,5-DIOXO-4,4-DIPHENYL-, ETHYL ESTER
P 6127
BRN 0762005
3-Ethoxycarbonyl-5,5-diphenyl hydantoin
DTXSID90149018
5-24-08-00381 (Beilstein Handbook Reference)
DTXCID9071509
ethyl 2,5-dioxo-4,4-diphenylimidazolidine-1-carboxylate
3-carbethoxy-5,5-diphenylhydantoin
P-6127
SCHEMBL11432635
WAOIWRAOVPQJKC-UHFFFAOYSA-N