1-ethylsulfanyl-N-(4-iodo-3-methyl-phenyl)methanimidothioic acid

Identification

Molecular formula

C₁₁H₁₄INS₂

CAS number

Not available

IUPAC name

1-ethylsulfanyl-N-(4-iodo-3-methyl-phenyl)methanimidothioic acid

State

At room temperature, 1-ethylsulfanyl-N-(4-iodo-3-methyl-phenyl)methanimidothioic acid is in a solid state, typically as a crystalline powder.

Melting point (Celsius)

155.00

Melting point (Kelvin)

428.15

Boiling point (Celsius)

373.15

Boiling point (Kelvin)

646.00

General information

Molecular weight

357.23g/mol

Molar mass

357.2000g/mol

Density

1.9000g/cm³

Appearence

1-Ethylsulfanyl-N-(4-iodo-3-methyl-phenyl)methanimidothioic acid appears as a crystalline solid. The compound can vary in color depending on purity and specific form, often appearing as yellow or off-white to brown crystalline powder.

Comment on solubility

Solubility of 1-ethylsulfanyl-N-(4-iodo-3-methyl-phenyl)methanimidothioic acid

The solubility of 1-ethylsulfanyl-N-(4-iodo-3-methyl-phenyl)methanimidothioic acid can be quite intriguing due to the presence of various functional groups that influence its behavior in different solvents. Here are some key points to consider:

Polar vs. Nonpolar Solvents: This compound likely exhibits better solubility in polar solvents due to the presence of the thioic acid group, which can form hydrogen bonds with solvent molecules.
Aromatic Influence: The iodo and methyl substituents on the phenyl ring can also affect solubility. Generally, substitutions on aromatic rings can either enhance or hinder solubility depending on the solvent used.
Temperature Effects: Solubility is often temperature-dependent. Increasing temperature may enhance the solubility of this compound in certain solvents, allowing for better dissolution.
Potential for Ionic Interaction: In some cases, the ionic nature of thioic acids when deprotonated can facilitate solubility in polar solvents, especially in aqueous conditions.

In conclusion, understanding the solubility of this compound involves considering its molecular structure and the solvent characteristics. As with many chemical compounds, experimentation will often be necessary to determine the exact solubility profile in various environments.

Interesting facts

Interesting Facts about 1-Ethylsulfanyl-N-(4-iodo-3-methyl-phenyl)methanimidothioic acid

1-Ethylsulfanyl-N-(4-iodo-3-methyl-phenyl)methanimidothioic acid is a fascinating compound that highlights the complexity and diversity found in organic chemistry. Here are some key points that shed light on its significance:

Unique Structure: This compound features a distinctive framework that includes a sulfonium group and a thioic acid moiety, showcasing the interplay of sulfur-containing functionalities in organic compounds.
Biological Relevance: The presence of iodine in its structure suggests potential applications in medicinal chemistry, as iodinated compounds often display enhanced biological activity. This makes it a point of interest in the study of pharmaceuticals.
Reactivity Potential: The thiol groups in this compound can engage in various chemical reactions, including nucleophilic substitutions and additions, making it a versatile building block in synthetic chemistry.
Research Applications: Due to its unique properties, research involving this compound can uncover new pathways for drug development, particularly in targeting specific biological processes.
Environmental Considerations: Compounds containing sulfur and iodine motifs may have implications in environmental chemistry, particularly regarding their stability and behavior in biological systems.

As the study of compounds like 1-ethylsulfanyl-N-(4-iodo-3-methyl-phenyl)methanimidothioic acid continues, scientists may unveil novel properties and applications that could significantly advance fields ranging from pharmaceuticals to environmental science. The compound exemplifies the intricate connections between structure, function, and potential utility in scientific research.