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Allantoin

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Identification
Molecular formula
C4H6N4O3
CAS number
97-59-6
IUPAC name
2-(3-methyl-2,4,5-trioxo-imidazolidin-1-yl)-N-phenyl-acetamide
State
State

Allantoin is typically solid at room temperature, existing as a crystalline powder.

Melting point (Celsius)
230.00
Melting point (Kelvin)
503.15
Boiling point (Celsius)
295.00
Boiling point (Kelvin)
568.15
General information
Molecular weight
158.12g/mol
Molar mass
158.1170g/mol
Density
1.4500g/cm3
Appearence

Allantoin typically appears as a white, odorless crystalline powder. It is often found in cosmetic products and topical formulations due to its skin-soothing properties.

Comment on solubility

Solubility of 2-(3-methyl-2,4,5-trioxo-imidazolidin-1-yl)-N-phenyl-acetamide

The solubility of 2-(3-methyl-2,4,5-trioxo-imidazolidin-1-yl)-N-phenyl-acetamide is an intriguing aspect of this compound, as it can be influenced by multiple factors:

  • Polarity: Given its structure, the compound may exhibit varying degrees of polarity, which can significantly impact its solubility in different solvents.
  • Temperature: Generally, an increase in temperature can enhance solubility for many solid compounds.
  • pH levels: The solubility may be affected by the pH of the environment, especially if the compound can exist in ionizable forms.
  • Solvent Type: The choice between polar solvents (like water) versus non-polar solvents (like hexane) will yield different solubility outcomes.

In summary, while empirical data may be limited, it is crucial to consider the overall molecular characteristics. The compound may exhibit moderate solubility in polar solvents due to the presence of both hydrophilic and hydrophobic regions. Further studies would clarify the solubility behavior across various conditions. Always remember when working with substances that "a substance is often shaped by its environment."

Interesting facts

Interesting Facts about 2-(3-methyl-2,4,5-trioxo-imidazolidin-1-yl)-N-phenyl-acetamide

This intriguing compound, known for its complex structure, presents various points of interest that highlight its importance in the realm of chemistry.

Chemical Structure and Significance

One of the remarkable features of this compound is its imidazolidinone core, which is known for:

  • Diverse Biological Activity: Compounds containing imidazolidinone structures are often linked to medicinal properties, making them potential candidates in drug discovery.
  • Multifunctional Usage: The presence of multiple functional groups facilitates various chemical reactions, making it useful in organic synthesis.

Applications

2-(3-methyl-2,4,5-trioxo-imidazolidin-1-yl)-N-phenyl-acetamide has significant applications within:

  • Pharmaceuticals: Due to its delicate balance of functionalities, it can be tailored to develop new therapeutic agents.
  • Agricultural Chemistry: The compound can serve as a lead structure for the synthesis of agrochemicals.

Research Perspectives

As a chemistry student, exploring this compound offers a glimpse into:

  • Structure-Activity Relationships (SAR): Understanding how changes in its structure impact biological reactivity can lead to more effective derivatives.
  • Innovative Synthesis Techniques: The compound's unique structure can encourage creative approaches in synthetic chemistry.

In conclusion, 2-(3-methyl-2,4,5-trioxo-imidazolidin-1-yl)-N-phenyl-acetamide is more than just a compound; it represents a valuable resource for exploring the intersections of biology, chemistry, and pharmacology. Its study could pave the way for significant advances in multiple scientific fields.

Synonyms
BRN 0815608
1-IMIDAZOLIDINEACETANILIDE, 3-METHYL-2,4,5-TRIOXO-
2211-53-2
DTXSID30176626
1-Methyl-3-phenylcarbamoylmethylimidazolidinetrione
3-Methyl-2,4,5-trioxo-1-imidazolidineacetanilide
1-Imidazolidineacetamide, 3-methyl-2,4,5-trioxo-N-phenyl-
DTXCID9099117
5-24-09-00055 (beilstein handbook reference)