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Glycodiazine

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Identification
Molecular formula
C12H12N2O2
CAS number
10465-91-7
IUPAC name
3-methyl-5-(p-tolylmethylene)imidazolidine-2,4-dione
State
State

At room temperature, this compound is in a solid state. It is commonly found as a crystalline powder, which can vary in color from white to slightly off-white.

Melting point (Celsius)
195.00
Melting point (Kelvin)
468.15
Boiling point (Celsius)
281.00
Boiling point (Kelvin)
554.15
General information
Molecular weight
229.25g/mol
Molar mass
229.2510g/mol
Density
1.2500g/cm3
Appearence

This compound is typically available as a white to off-white crystalline powder. Its appearance can vary slightly due to different formulation methods and purity levels.

Comment on solubility

Solubility of 3-methyl-5-(p-tolylmethylene)imidazolidine-2,4-dione

The solubility of 3-methyl-5-(p-tolylmethylene)imidazolidine-2,4-dione, often referred to as a versatile chemical compound, can be influenced by various factors. This compound is primarily known for its unique structure, which significantly affects its interaction with solvents. Below are key considerations regarding its solubility:

  • Solvent Polarity: The solubility of the compound typically increases in polar solvents such as water and alcohols, owing to its functional groups that can interact favorably with polar molecules.
  • Temperature Factors: As with many compounds, solubility may increase with rising temperatures, enhancing the dissolution process.
  • pH Sensitivity: The solubility can be affected by the pH of the solution, as ionizable groups may behave differently in acidic versus basic environments.
  • Crystal Structure: The crystalline form of the compound may also play a role in solubility; different polymorphs can exhibit varying solubility characteristics.

In summary, the solubility of 3-methyl-5-(p-tolylmethylene)imidazolidine-2,4-dione is not straightforward and is contingent upon the specific conditions under which it is analyzed. Understanding its solubility behavior is crucial for applications in synthesis and formulation processes.

Interesting facts

Interesting Facts about 3-methyl-5-(p-tolylmethylene)imidazolidine-2,4-dione

This compound, known as 3-methyl-5-(p-tolylmethylene)imidazolidine-2,4-dione, is a fascinating member of the imidazolidine family that showcases remarkable structural features and potential applications in various fields. Here are some key points to consider:

  • Structure Significance: The presence of both the methyl group and the p-tolylmethylene moiety allows for unique stereochemical configurations that may influence the compound's reactivity and interactions.
  • Biological Relevance: Compounds in the imidazolidine class, including this one, have been studied for their potential biological activity, with applications that may range from medicinal chemistry to agrochemicals.
  • Potential Applications: Research indicates that such compounds may act as enzyme inhibitors or exhibit anti-inflammatory properties, making them of interest in pharmacological studies.
  • Synthetic Pathways: The synthesis of 3-methyl-5-(p-tolylmethylene)imidazolidine-2,4-dione often involves the condensation of primary amines and diones, which can vary greatly based on the desired substituents and reaction conditions.

As chemists delve deeper into the study of this compound, they often remark that “the beauty of organic chemistry lies not just in the compounds we create, but in the intricate dance of atoms that make up their very essence.” This is particularly true for compounds like 3-methyl-5-(p-tolylmethylene)imidazolidine-2,4-dione, where the interplay of structure and function beckons further exploration.

In summary, 3-methyl-5-(p-tolylmethylene)imidazolidine-2,4-dione stands as a compelling example of how subtle changes in molecular structure can lead to diverse and intriguing possibilities in science.

Synonyms
SCHEMBL15302367
UUGULLSNDIRBJI-UHFFFAOYSA-N
AKOS004901376
5-(4-methylbenzylidene)-3-methylhydantoin