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

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Identification
Molecular formula
C17H13ClN2OS
CAS number
145858-04-2
IUPAC name
5-[(4-chlorophenyl)methylene]-3-(p-tolyl)-2-sulfanyl-imidazol-4-one
State
State

At room temperature, this compound is typically in a solid state, specifically as a crystalline powder.

Melting point (Celsius)
220.00
Melting point (Kelvin)
493.15
Boiling point (Celsius)
420.00
Boiling point (Kelvin)
693.15
General information
Molecular weight
328.82g/mol
Molar mass
328.8400g/mol
Density
1.3500g/cm3
Appearence

This compound typically appears as a white to off-white crystalline powder. Its crystalline nature allows for a consistent structure, contributing to distinct melting and boiling points.

Comment on solubility

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

The solubility of 5-[(4-chlorophenyl)methylene]-3-(p-tolyl)-2-sulfanyl-imidazol-4-one in various solvents is influenced by its molecular structure and functional groups. Understanding the solubility of this compound can be pivotal for its applications in pharmaceuticals and material sciences.

Factors Affecting Solubility

  • Molecular Polarity: The presence of polar functional groups may enhance solubility in polar solvents, while non-polar sections may favor solubility in non-polar solvents.
  • Temperature: Solubility generally increases with temperature; knowing how this compound behaves can affect its practical use in solutions.
  • pH Levels: The ionization state of the molecule may change with pH, affecting its solubility in aqueous environments.

While comprehensive data on this specific compound's solubility might be limited, one can categorize potential solubility characteristics based on similar structures:

  • Soluble in organic solvents: Compounds with larger aromatic systems may appear to have increased solubility in organic solvents such as dichloromethane or ethanol.
  • Limited solubility in water: Given the non-polar structures, one might anticipate lower water solubility due to hydrophobic nature.

In conclusion, understanding the solubility of 5-[(4-chlorophenyl)methylene]-3-(p-tolyl)-2-sulfanyl-imidazol-4-one is essential not only for its chemical handling but also for maximizing its efficacy in various applications. As the popular phrase goes, "Like dissolves like," emphasizing the importance of matching solvent and solute polarities to enhance solubility outcomes.

Interesting facts

Interesting Facts about 5-[(4-chlorophenyl)methylene]-3-(p-tolyl)-2-sulfanyl-imidazol-4-one

This intriguing compound showcases the fascinating world of imidazole derivatives, which are often noted for their biological significance and utility in medicinal chemistry. Here are some captivating aspects of this compound:

  • Pharmacological Potential: Many imidazole derivatives, including this compound, exhibit a range of biological activities, making them of great interest in drug design and development. They can act as anti-inflammatory agents, antifungals, and even as anti-cancer agents.
  • Substituent Effects: The presence of both 4-chlorophenyl and p-tolyl groups significantly impacts the compound's chemical properties and reactivity. Chlorine atoms can enhance lipophilicity, potentially aiding in membrane penetration of biological cells.
  • Mechanistic Insights: Compounds like this one are often investigated for their ability to interfere with specific enzyme pathways. Understanding how they work at the molecular level can reveal new therapeutic targets.
  • Synthetic Pathways: The synthesis of imidazole derivatives can involve multi-step reactions, providing a rich ground for exploring organic synthesis techniques and methodologies.

In conclusion, 5-[(4-chlorophenyl)methylene]-3-(p-tolyl)-2-sulfanyl-imidazol-4-one represents a sophisticated balance between structure and function. As researchers continue to explore its properties, it holds promise for future breakthroughs in chemical research and pharmaceutical applications.