N-(3-Chloro-4-iodophenyl)-1-ethylsulfanyl-methanimidothioic acid

Identification

Molecular formula

C₁₀H₉ClINS₂

CAS number

1211589-94-7

IUPAC name

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

State

The compound is a solid at room temperature, typically found in a crystalline form.

Melting point (Celsius)

154.00

Melting point (Kelvin)

427.15

Boiling point (Celsius)

370.00

Boiling point (Kelvin)

643.15

General information

Molecular weight

364.63g/mol

Molar mass

364.6300g/mol

Density

1.6800g/cm³

Appearence

The compound typically appears as a crystalline solid with an off-white to yellowish color. It may have a slight odor characteristic of thio compounds.

Comment on solubility

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

N-(3-chloro-4-iodo-phenyl)-1-ethylsulfanyl-methanimidothioic acid is a unique compound with a complex structure that impacts its solubility profile. Its solubility can be influenced by several factors:

Polarity: The presence of functional groups, particularly the thioic acid group, often contributes to the compound's overall polarity. This can lead to increased solubility in polar solvents like water.
Hydrogen bonding: The potential for hydrogen bonding with solvent molecules can significantly enhance solubility, especially in aqueous environments.
Temperature: Like many organic compounds, the solubility of N-(3-chloro-4-iodo-phenyl)-1-ethylsulfanyl-methanimidothioic acid can vary with temperature. As temperature increases, solubility generally increases due to enhanced kinetic energy.
Solvent type: Solubility is also affected by the choice of solvent; it may dissolve readily in dimethyl sulfoxide (DMSO) or other organic solvents while showing limited solubility in nonpolar solvents.

In conclusion, the solubility of N-(3-chloro-4-iodo-phenyl)-1-ethylsulfanyl-methanimidothioic acid is a multifaceted phenomenon influenced by its unique chemical structure and environmental conditions. Understanding these factors is crucial for its effective application in various fields.

Interesting facts

Interesting Facts About N-(3-chloro-4-iodo-phenyl)-1-ethylsulfanyl-methanimidothioic acid

N-(3-chloro-4-iodo-phenyl)-1-ethylsulfanyl-methanimidothioic acid is a fascinating compound with significant relevance in various fields of chemistry. Here are some intriguing highlights about this compound:

Pharmaceutical Potential: This compound holds promise in medicinal chemistry due to its unique structure. The presence of halogen substituents (chlorine and iodine) often plays a critical role in biological activity, making it a possible candidate for drug development.
Thioic Acid Derivative: As a derivative of thioic acid, it exhibits unique properties that can lead to novel chemical reactivity. The thioamide functional group is known for its ability to participate in a variety of chemical reactions, including synthesis pathways in organic chemistry.
Synthetic Versatility: The compound's synthetic route opens up various avenues for chemists. Its multi-functional groups allow for further modifications, making it a versatile substrate for creating more complex molecules.
Environmental Impact: Compounds containing iodine and chlorine have implications in environmental chemistry. Their effects on ecosystems, especially when considering their persistence and potential bioaccumulation, are crucial areas of study.
Research Opportunities: The compound is an excellent subject for research in fields such as materials science and nanotechnology, given its potential to interact with other materials at the molecular level.

In conclusion, N-(3-chloro-4-iodo-phenyl)-1-ethylsulfanyl-methanimidothioic acid stands out as a compound with promising applications in medicinal chemistry, materials science, and environmental studies. As chemists continue to explore its unique features, it may pave the way for new discoveries and innovations in these fields. As one renowned chemist once stated, "The discovery of a new compound is not the end; it is merely the beginning of a deeper understanding of nature."