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1-[(4-chlorophenyl)methylsulfanyl]-N-(4-iodophenyl)methanimidothioic acid

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Identification
Molecular formula
C14H11ClINS2
CAS number
104204-13-7
IUPAC name
1-[(4-chlorophenyl)methylsulfanyl]-N-(4-iodophenyl)methanimidothioic acid
State
State

This compound is typically a solid at room temperature with a crystalline structure. It is stable under normal conditions.

Melting point (Celsius)
152.30
Melting point (Kelvin)
425.45
Boiling point (Celsius)
536.70
Boiling point (Kelvin)
809.85
General information
Molecular weight
424.84g/mol
Molar mass
424.8410g/mol
Density
1.8000g/cm3
Appearence

This compound is a solid at room temperature. It typically presents as a crystalline solid, which may vary in color depending on purity and processing methods.

Comment on solubility

Solubility of 1-[(4-chlorophenyl)methylsulfanyl]-N-(4-iodophenyl)methanimidothioic acid

This compound exhibits intriguing solubility characteristics due to its complex molecular structure. The presence of both chlorinated and iodinated phenyl groups contributes to its overall polarity, which can influence its solubility in various solvents. Here are some key considerations regarding its solubility:

  • In Polar Solvents: This compound is more likely to be soluble in polar solvents such as water and alcohols due to the functionality of the thioic acid moiety.
  • In Non-Polar Solvents: Conversely, the larger, non-polar aromatic rings may hinder solubility in non-polar solvents, suggesting a selective solubility profile.
  • Temperature Dependency: As with many chemical compounds, solubility may increase with temperature, promoting better dissolution in mixed solvents.
  • pH Effects: The presence of the thioic acid functional group may lead to variable solubility at different pH levels, where ionization could significantly enhance solubility.

In summary, the solubility of 1-[(4-chlorophenyl)methylsulfanyl]-N-(4-iodophenyl)methanimidothioic acid is influenced by its unique chemical properties and the nature of the solvent used. Understanding these solubility patterns is crucial for the development and application of this compound in various chemical processes.

Interesting facts

Interesting Facts about 1-[(4-chlorophenyl)methylsulfanyl]-N-(4-iodophenyl)methanimidothioic acid

This intriguing compound, often referred to in the scientific community for its unique structure and potential applications, is a fascinating example of the intersection between organic chemistry and medicinal research. Its molecular design incorporates both a chlorophenyl and an iodophenyl moiety, which can significantly influence its chemical behavior and biological activity.

Key Characteristics

  • Diverse Applications: This compound holds promise in various fields such as medicinal chemistry, particularly in the development of pharmaceuticals due to its potential bioactivity.
  • Structural Complexity: The sulfur atom in the thioic acid group adds reactivity and potentially enhances interactions with biological targets, making it a subject of interest for further study.
  • Halogen Influence: The presence of halogens (chlorine and iodine) in its structure often relates to altered physicochemical properties, which can impact the compound's interaction with receptors in biological systems.

Researchers continue to explore the implications of these structural features, often quoting that "the variations in substituents can lead to vast differences in activity." Such variation emphasizes the importance of chemical modifications in drug design and development.

Scientific Research and Potential

Due to its complex structure, ongoing studies may investigate its:

  • Antitumor properties
  • Antimicrobial efficacy
  • Potential role in the treatment of various diseases influenced by the biological pathways this compound may affect

As the field of medicinal chemistry advances, compounds like 1-[(4-chlorophenyl)methylsulfanyl]-N-(4-iodophenyl)methanimidothioic acid highlight the importance of structure-activity relationships in drug development, inspiring chemists and biologists alike to delve deeper into the world of chemical compounds.