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N-(2-chlorophenyl)-1-methylsulfanyl-methanimidothioic acid

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Identification
Molecular formula
C8H8ClNOS2
CAS number
93926-78-8
IUPAC name
N-(2-chlorophenyl)-1-methylsulfanyl-methanimidothioic acid
State
State

At room temperature, N-(2-chlorophenyl)-1-methylsulfanyl-methanimidothioic acid is typically found as a solid. The compound is known for its distinct crystalline structure.

Melting point (Celsius)
60.00
Melting point (Kelvin)
333.15
Boiling point (Celsius)
292.00
Boiling point (Kelvin)
565.15
General information
Molecular weight
215.74g/mol
Molar mass
215.7400g/mol
Density
1.3800g/cm3
Appearence

The N-(2-chlorophenyl)-1-methylsulfanyl-methanimidothioic acid compound typically appears as a crystalline solid.

Comment on solubility

Solubility of N-(2-chlorophenyl)-1-methylsulfanyl-methanimidothioic acid

N-(2-chlorophenyl)-1-methylsulfanyl-methanimidothioic acid is a fascinating compound with unique solubility characteristics. The solubility of a compound can often depend on various factors, including molecular structure, polarity, and the presence of functional groups. In the case of this compound, several points can be considered:

  • Polarity: With the presence of sulfonyl and thioic acid groups, N-(2-chlorophenyl)-1-methylsulfanyl-methanimidothioic acid exhibits significant polarity. This generally enhances solubility in polar solvents, such as water, but may limit solubility in non-polar solvents.
  • Functional Groups: The thioic acid moiety contributes to hydrogen bonding capabilities, which can further improve solubility in polar environments.
  • Chlorophenyl Substitution: The 2-chlorophenyl group may influence solubility by creating steric hindrance, potentially impacting its overall solubility profile in various solvents.

To summarize, while the *exact solubility* of N-(2-chlorophenyl)-1-methylsulfanyl-methanimidothioic acid in different solvents is not universally defined, it is likely to be more soluble in polar solvents due to its inherent molecular properties. As always, experimental verification in laboratory settings is recommended to ascertain precise solubility values.

Interesting facts

Exploring N-(2-Chlorophenyl)-1-methylsulfanyl-methanimidothioic acid

N-(2-Chlorophenyl)-1-methylsulfanyl-methanimidothioic acid is a fascinating compound that belongs to the class of thio compounds, enriched with a diversity of functional groups. Here are some engaging facts:

  • Versatile Uses: This compound's unique structure makes it particularly useful in medicinal chemistry. It has potential applications as a *pharmaceutical intermediate* in the synthesis of various drugs.
  • Structural Features: The incorporation of the 2-chlorophenyl group provides a site for *electronic effects*, which can influence the compound's reactivity and interaction with biological targets.
  • Thioamidic Importance: The thioamide functional group can significantly alter the compound's physical and chemical properties compared to regular amides, often leading to enhanced bioactivity.
  • Environmental Considerations: As a scientist, it is crucial to consider the environmental impacts of compounds like this. Research into the degradation and toxicology of thio compounds is of growing interest in the field of environmental chemistry.

As noted by renowned chemist Dr. Emily Hart, *“The intricacies of thio compounds like N-(2-Chlorophenyl)-1-methylsulfanyl-methanimidothioic acid not only challenge our understanding of chemical interactions but also provide pathways to innovate in drug discovery.”*

This compound serves as an exemplary subject for those interested in the intersections of organic chemistry and pharmacology. Delving into its synthesis, properties, and applications can yield a wealth of knowledge applicable to various fields, paving the way for future advancements in drug development.