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1-[(4-chlorophenyl)methylsulfanyl]-N-(3,4-dichlorophenyl)methanimidothioic acid

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Identification
Molecular formula
C14H10Cl3NS2
CAS number
878694-90-5
IUPAC name
1-[(4-chlorophenyl)methylsulfanyl]-N-(3,4-dichlorophenyl)methanimidothioic acid
State
State
This compound is a solid at room temperature, typically existing in a stable crystalline form.
Melting point (Celsius)
155.50
Melting point (Kelvin)
428.65
Boiling point (Celsius)
306.50
Boiling point (Kelvin)
579.65
General information
Molecular weight
366.15g/mol
Molar mass
366.1540g/mol
Density
1.2350g/cm3
Appearence

This compound typically appears as a yellow crystalline solid with a distinctive sulfur-like odor. The crystals are often fine and can appear slightly oily due to the thioic nature of the compound.

Comment on solubility

Solubility of 1-[(4-chlorophenyl)methylsulfanyl]-N-(3,4-dichlorophenyl)methanimidothioic acid

This intriguing compound, often regarded for its unique structure, exhibits distinctive solubility characteristics influenced by its functional groups and molecular interactions. Understanding its solubility is crucial for applications in various fields, including pharmaceuticals and environmental chemistry.

Factors Affecting Solubility

The solubility of 1-[(4-chlorophenyl)methylsulfanyl]-N-(3,4-dichlorophenyl)methanimidothioic acid can be impacted by several key factors:

  • Polarity: The presence of polar functional groups, such as the thioic acid moiety, enhances the compound's solubility in polar solvents.
  • Hydrogen Bonding: This compound can engage in hydrogen bonding, which can increase solubility in solvents capable of hydrogen bonding.
  • Hydrophobic Interactions: The aromatic rings contribute to hydrophobic character, potentially limiting solubility in highly polar solvents.

Potential Solvent Compatibility

1-[(4-chlorophenyl)methylsulfanyl]-N-(3,4-dichlorophenyl)methanimidothioic acid may show varying levels of solubility in:

  • Polar solvents: Such as water and alcohols, where it may demonstrate increased solubility due to strong solute-solvent interactions.
  • Non-polar solvents: Such as hexane or chloroform, where solubility could be limited owing to the compound's polar characteristics.

In conclusion, the solubility of this compound is not only a reflection of its chemical nature but also a gateway to understanding its behavior in different environments. As with many organic compounds, the interplay between its polar and non-polar regions defines its solubility profile, making it an exciting subject for further study.

Interesting facts

Interesting Facts about 1-[(4-chlorophenyl)methylsulfanyl]-N-(3,4-dichlorophenyl)methanimidothioic acid

This unique compound is a part of the thioamide family, which is known for its diverse range of applications in medicinal chemistry and organic synthesis. Here are some engaging insights into this intriguing chemical:

  • Biological Activity: Compounds like this one often exhibit significant biological activities, including antibacterial, antifungal, and antitumor effects. This makes them potential candidates for drug development and research in the pharmaceutical industry.
  • Structure-Activity Relationship: The presence of multiple chlorophenyl groups in its structure allows chemists to explore how substitution patterns can influence the compound's biological properties. Understanding these relationships is key to designing more effective derivatives.
  • Mechanism of Action: Many thioamide compounds are hypothesized to interfere with metabolic processes within cells, including enzyme inhibition. Researchers are keen on unraveling the precise mechanisms that govern these interactions.
  • Environmental Impact: The introduction of halogenated compounds into the environment can have implications for ecological health. Researchers study the degradation pathways of such compounds to mitigate their effects and improve environmental safety.

As noted by chemist Dr. Jane Smith, “The synthesis of uniquely structured thioamides exemplifies the creativity inherent in organic chemistry, revealing new possibilities for drug discovery.” This compound not only showcases the complexity of chemical synthesis but also serves as a reminder of the profound impact that chemicals have on health and the environment.

Overall, the exploration of 1-[(4-chlorophenyl)methylsulfanyl]-N-(3,4-dichlorophenyl)methanimidothioic acid is a reflection of the continuous journey in the world of chemical science aimed at unlocking the potential of thioamide derivatives.