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N-(4-Chlorophenyl)-1-methylsulfanylmethanimidothioic acid

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Identification
Molecular formula
C9H10ClNOS2
CAS number
null
IUPAC name
N-(4-chlorophenyl)-1-methylsulfanyl-methanimidothioic acid
State
State

This compound is typically a solid at room temperature.

Melting point (Celsius)
165.20
Melting point (Kelvin)
438.40
Boiling point (Celsius)
292.50
Boiling point (Kelvin)
565.70
General information
Molecular weight
232.75g/mol
Molar mass
232.7500g/mol
Density
1.4800g/cm3
Appearence

The compound appears as a yellow crystalline powder. It is typically characterized by its distinctive color and crystalline form.

Comment on solubility

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

N-(4-chlorophenyl)-1-methylsulfanyl-methanimidothioic acid is a complex chemical compound with a unique structure that influences its solubility characteristics. Understanding the solubility of this compound involves several crucial factors:

  • Polarity: The presence of polar functional groups in the compound can enhance its solubility in polar solvents like water, while non-polar regions may favor solubility in organic solvents.
  • Hydrogen Bonding: If the compound can engage in hydrogen bonding with solvents, it typically increases solubility significantly. Conversely, a lack of such interactions can lead to lower solubility.
  • Temperature: As is common with many chemical compounds, solubility can increase with temperature. Experiments can help determine the specific solubility behavior at various temperatures.
  • pH Level: The pH of the solution can also play a critical role, especially if the compound can be ionized in the presence of acids or bases.

In practical terms, while specific solubility data for this compound may be limited, it is essential to consider the above factors when predicting its behavior in different solvents.

To summarize, the solubility of N-(4-chlorophenyl)-1-methylsulfanyl-methanimidothioic acid depends on:

  1. Its chemical structure and functional groups.
  2. The solvent's polarity and intermolecular interactions.
  3. External conditions such as temperature and pH.

Through careful experimentation and analysis, researchers can gain valuable insights into the solubility profile of this intriguing compound.

Interesting facts

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

N-(4-chlorophenyl)-1-methylsulfanyl-methanimidothioic acid is a fascinating compound noteworthy for its uniqueness and applications in various fields. Here are some engaging facts to consider:

  • Structural Complexity: This compound showcases a complex molecular structure, which includes a chlorophenyl group, contributing to its distinctive properties and reactivity.
  • Reactiveness: The presence of the methanimidothioic acid moiety provides this compound with enhanced reactivity. This functionality is often associated with biological activity, making it a subject of interest in medicinal chemistry.
  • Biological Relevance: Due to its sulfur-containing structure, compounds similar to N-(4-chlorophenyl)-1-methylsulfanyl-methanimidothioic acid are often explored for their potential therapeutic applications, particularly in the development of pharmaceuticals that target specific biological pathways.
  • Environmental Impact: The chlorinated component raises discussions about environmental sustainability and safety. Chlorinated compounds can pose risks to ecosystems, highlighting the importance of studying the environmental fate of such chemicals.
  • Synthesis and Derivatives: The synthesis of this compound can serve as a starting point for creating various derivatives. Chemists are often excited about modifying existing compounds to enhance their properties — thus extending their applications.
  • Historical Context: Compounds like this have a rich history in organic synthesis, dating back to the evolution of amine chemistry. They often serve as precursors in the formation of even more complex molecules.

In summary, N-(4-chlorophenyl)-1-methylsulfanyl-methanimidothioic acid is more than just a chemical compound; it represents a crossroads of chemistry, biology, and environmental science, making it a valuable subject for ongoing research and exploration.