5-[(2-Chlorophenyl)methylene]-3-phenyl-2-sulfanyl-imidazol-4-one

Identification

Molecular formula

C₁₆H₁₁ClN₂OS

CAS number

100846-89-9

IUPAC name

5-[(2-chlorophenyl)methylene]-3-phenyl-2-sulfanyl-imidazol-4-one

State

This compound is typically a solid at room temperature, characterized by a stable crystalline structure. Its solid state makes it amenable for handling in various applications, including in laboratory research and chemical analysis.

Melting point (Celsius)

208.00

Melting point (Kelvin)

481.15

Boiling point (Celsius)

548.20

Boiling point (Kelvin)

821.40

General information

Molecular weight

330.79g/mol

Molar mass

330.8100g/mol

Density

1.3395g/cm³

Appearence

5-[(2-Chlorophenyl)methylene]-3-phenyl-2-sulfanyl-imidazol-4-one typically appears as a crystalline solid. It may exhibit varying colors depending on the quality and purity of the sample, ranging from white to light yellow.

Comment on solubility

Solubility of 5-[(2-chlorophenyl)methylene]-3-phenyl-2-sulfanyl-imidazol-4-one

The solubility of 5-[(2-chlorophenyl)methylene]-3-phenyl-2-sulfanyl-imidazol-4-one can depend on various factors, including the nature of the solvent, temperature, and the compound's structural characteristics. This compound features complex aromatic and sulfur-containing moieties, which may influence its solubility behavior.

Key Points on Solubility:

Polarity: The presence of polar groups may increase solubility in polar solvents such as water, while non-polar groups tend to favor solubility in organic solvents.
Hydrogen Bonding: Potential for hydrogen bonding can significantly impact solubility; hence, assessing functional groups is vital.
Temperature Dependence: Solubility typically increases with temperature for many compounds, but specific behavior should be experimentally determined.
pH Sensitivity: The ionization of the compound at different pH levels can modify solubility; thus, understanding the pH of the environment is crucial.

In summary, the solubility of 5-[(2-chlorophenyl)methylene]-3-phenyl-2-sulfanyl-imidazol-4-one is likely to be multifaceted and should be evaluated in a systematic manner under controlled conditions to obtain reliable data. The overarching takeaway is that while predicting solubility can be complex, it is a fundamental property that can be explored through a combination of theoretical knowledge and empirical investigation.

Interesting facts

Interesting Facts About 5-[(2-Chlorophenyl)methylene]-3-phenyl-2-sulfanyl-imidazol-4-one

This compound, with its intricate structure, belongs to the family of imidazoles, which are well-known in medicinal chemistry for their versatile biological activity. The presence of both the 2-chlorophenyl and 3-phenyl groups enhances its potential reactivity and interaction with biological targets.

Here are a few intriguing insights about this particular imidazole derivative:

Unique Functional Groups: The compound features a thiol (-SH) group, which imparts significant nucleophilic properties, allowing it to participate in various chemical reactions, such as disulfide bond formation, and redox chemistry.
Biological Relevance: Compounds containing imidazole rings have been widely researched for their roles in drug design. They frequently exhibit properties such as antibacterial, antifungal, and anti-cancer activities.
Chlorine Substitution: The presence of the chlorine atom increases the compound's lipophilicity and can enhance its binding affinity to biological receptors, improving its efficacy as a pharmaceutical agent.

As a scientist or chemistry enthusiast exploring this compound, one can appreciate its potential applications in drug development and optimization. According to a renowned chemist, "Understanding the subtle changes in chemical structure can lead to discovering new therapeutic avenues." This statement emphasizes the importance of structural variations in designing effective medicines.

In summary, 5-[(2-chlorophenyl)methylene]-3-phenyl-2-sulfanyl-imidazol-4-one exemplifies the rich tapestry of organic chemistry where modifications can significantly influence biological activity, making it a promising candidate for future pharmacological studies.