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Identification
Molecular formula
C12H11ClN2O2S
CAS number
not known
IUPAC name
4-[(4-chlorophenoxy)methyl]-4-methyl-2-sulfanyl-1H-imidazol-5-one
State
State

This compound is typically a solid at room temperature, owing to its molecular structure and weight which leads to significant intermolecular forces.

Melting point (Celsius)
170.00
Melting point (Kelvin)
443.15
Boiling point (Celsius)
350.00
Boiling point (Kelvin)
623.15
General information
Molecular weight
268.74g/mol
Molar mass
268.7400g/mol
Density
1.4000g/cm3
Appearence

4-[(4-chlorophenoxy)methyl]-4-methyl-2-sulfanyl-1H-imidazol-5-one typically appears as a solid substance. The solid is generally crystalline in nature with a possible off-white color, owing to its chemical structure and composition.

Comment on solubility

Solubility of 4-[(4-chlorophenoxy)methyl]-4-methyl-2-sulfanyl-1H-imidazol-5-one

The solubility of 4-[(4-chlorophenoxy)methyl]-4-methyl-2-sulfanyl-1H-imidazol-5-one is an important characteristic that defines its behavior in various solvents. Understanding the solubility of this compound is essential for its practical applications and formulations.

Key points about the solubility of this compound include:

  • Polarity Factors: The presence of the -chlorophenoxy group suggests a degree of polarity, which can influence solubility in polar solvents such as water and alcohol.
  • Hydrophobic Interactions: The methyl group and other non-polar sections may lead to decreased solubility in highly polar solvents, making the compound potentially more soluble in organic solvents like ethanol or dimethyl sulfoxide (DMSO).
  • pH Dependence: As an imidazole derivative, its solubility might also be affected by pH, particularly in aqueous solutions, where protonation may enhance solubility.

It is notable that solubility can vary widely depending on specific conditions such as temperature, the presence of salts, and solvent mixtures. Thus, careful experimentation is essential to determine the most suitable solvent for this compound. Ultimately, ∆these factors collectively make understanding solubility both intriguing and complex.

Interesting facts

Interesting Facts about 4-[(4-chlorophenoxy)methyl]-4-methyl-2-sulfanyl-1H-imidazol-5-one

This compound, known for its complex structure and unique properties, is a fascinating subject of study in the field of medicinal chemistry. Here are some engaging aspects of this compound:

  • Structural Diversity: The presence of both a chlorophenoxy group and a sulfanyl moiety introduces a significant level of complexity, allowing for interesting interactions with biological targets.
  • Biological Relevance: Compounds similar to this one have been investigated for their potential therapeutic applications. They may exhibit pharmacological activities that could be beneficial in various therapeutic areas such as anti-inflammatory or antifungal treatments.
  • Synthetic Pathways: The synthesis of this compound can involve multiple steps, including the introduction of the sulfanyl group and the chlorophenoxy substitution, making it a good candidate for studies on synthetic methodologies.
  • Pharmacophore Identification: Scientists often analyze the structure of this compound to identify its pharmacophore, which is critical for understanding how it interacts with different biological molecules.
  • Compound Stability: The imidazole ring is notable for its stability and ability to participate in various chemical reactions, making it a key component in many pharmaceutical compounds.
  • Multifunctional Roles: The factors contributing to this compound's potential include its ability to act as a ligand or as an inhibitor, providing versatility in drug discovery processes.

As scientists and chemists continue to explore compounds like 4-[(4-chlorophenoxy)methyl]-4-methyl-2-sulfanyl-1H-imidazol-5-one, they hope to unveil new pathways for drug development and therapeutic interventions. The compound serves as a reminder of the intricacies within the chemical world and the ongoing quest to harness these structures for human health.