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3-benzoyl-2-mercapto-4H-imidazol-5-one

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Identification
Molecular formula
C10H6N2O2S
CAS number
76039-75-1
IUPAC name
3-benzoyl-2-sulfanyl-4H-imidazol-5-one
State
State

At room temperature, the compound is in a solid state, characterized often by its crystalline structure.

Melting point (Celsius)
210.00
Melting point (Kelvin)
483.15
Boiling point (Celsius)
480.00
Boiling point (Kelvin)
753.15
General information
Molecular weight
218.25g/mol
Molar mass
218.2500g/mol
Density
1.3447g/cm3
Appearence

The compound is typically a crystalline solid. The exact color can vary but is often white to off-white depending on the purity and form of the compound.

Comment on solubility

Solubility of 3-benzoyl-2-sulfanyl-4H-imidazol-5-one

The solubility of 3-benzoyl-2-sulfanyl-4H-imidazol-5-one is a noteworthy characteristic that can significantly influence its applications in various chemical processes. Understanding its solubility properties involves several key factors:

  • Polarity: The presence of the benzoyl group contributes to the overall polarity of the compound, which can affect its interaction with solvents.
  • Hydrophilicity vs. Hydrophobicity: Due to the nature of the imidazole ring and the sulfhyl (–SH) group, this compound exhibits a balance between hydrophilic and hydrophobic behavior.
  • Solvent Choice: It is likely to be more soluble in organic solvents than in water. Popular solvents for this compound might include:
    • Dimethyl sulfoxide (DMSO)
    • Acetone
    • Ethanol

It is essential to recognize that solubility can vary with temperature and concentration. Investing in solubility tests under different conditions can provide more reliable data on its overall behavior in various environments. This information is crucial when considering pharmaceutical formulations or chemical synthesis pathways where the solubility of a compound plays a vital role in its efficacy and reactivity.

Interesting facts

Interesting Facts about 3-benzoyl-2-sulfanyl-4H-imidazol-5-one

3-benzoyl-2-sulfanyl-4H-imidazol-5-one is a fascinating compound that falls under the category of imidazole derivatives, a class known for their biological significance and versatile applications in medicinal chemistry. This particular compound features both a benzoyl group and a sulfanyl group, which endow it with unique properties that make it a subject of interest in various fields.

Key Features

  • Biological Activity: Compounds like 3-benzoyl-2-sulfanyl-4H-imidazol-5-one are being investigated for their antimicrobial, antifungal, and antioxidant properties. The imidazole ring is known for its role in many naturally occurring substances, including histidine and various alkaloids.
  • Versatility: This compound can serve as a starting material or a building block in organic synthesis, particularly in the development of pharmaceutical agents.
  • Reactivity: The sulfenyl group in the compound adds a level of reactivity that is of interest to chemists, as it can participate in various chemical transformations, leading to the synthesis of new and complex molecular architectures.

Research and Applications

Recent studies have shown potential for new formulations based on 3-benzoyl-2-sulfanyl-4H-imidazol-5-one to address drug resistance in bacteria and fungi. By exploiting its structural characteristics, researchers aim to create novel therapeutic agents that are both effective and have reduced side effects.

In addition, the compound's ability to form stable complexes with metal ions opens avenues for research into catalytic processes and material science, including the development of new sensors and catalysts.

In summary, 3-benzoyl-2-sulfanyl-4H-imidazol-5-one exemplifies the intriguing world of chemical compounds, showcasing the interplay between structure and function that is fundamental to chemical research. With ongoing studies, who knows what new discoveries await in unlocking the full potential of this compound!