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

Identification

Molecular formula

C₁₀H₉ClIN₂O₂S₂

CAS number

Not available

IUPAC name

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

State

At room temperature, this compound is a solid. Its crystalline form is yellow to beige in color.

Melting point (Celsius)

98.00

Melting point (Kelvin)

371.15

Boiling point (Celsius)

257.00

Boiling point (Kelvin)

530.15

General information

Molecular weight

356.09g/mol

Molar mass

356.0900g/mol

Density

1.7800g/cm³

Appearence

This compound appears as a yellow to beige crystalline solid. The crystalline nature indicates its solid state under ambient conditions.

Comment on solubility

Solubility Characteristics

The compound N-(3-chloro-4-iodo-phenyl)-1-ethoxycarbonylsulfanyl-methanimidothioic acid exhibits unique solubility traits that are influenced by its structural composition. Understanding its solubility is essential for determining its potential applications and behavior in various environments.

Generally, the solubility of this compound can be assessed based on several key factors:

Polarity: The presence of polar functional groups such as the carbonyl and thioic acid may impart a certain degree of polarity, facilitating solubility in polar solvents like water.
Hydrophobic Interactions: The phenyl ring along with halogen substitutions can enhance hydrophobic interactions, which might limit solubility in highly polar solvents.
Solvent Compatibility: Aqueous solubility may be supported in mixed solvent systems, depending on the solvent composition. For example, mixing water with organic solvents could influence the solubility behavior.
pH Influence: The acidic nature of the thioic acid portion suggests that solubility could vary significantly with pH changes, potentially being more soluble in alkaline conditions due to deprotonation.

In conclusion, while N-(3-chloro-4-iodo-phenyl)-1-ethoxycarbonylsulfanyl-methanimidothioic acid demonstrates potential for solubility in various environments, it is crucial to conduct detailed experiments to confirm solubility behaviors under specific conditions. As the saying goes, "Solubility is key to reactivity!"

Interesting facts

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

N-(3-chloro-4-iodo-phenyl)-1-ethoxycarbonylsulfanyl-methanimidothioic acid is a fascinating compound that captivates the attention of chemists through its intriguing structure and potential applications. Here are some notable aspects:

Functional Diversity: This compound features a complex array of functional groups, including a thioic acid, which highlights its potential as a versatile building block in organic synthesis.
Halogen Influence: The presence of both chlorine and iodine atoms introduces unique reactivity patterns that can facilitate *substitution reactions*, often leading to remarkable alterations in chemical behavior.
Biological Implications: Compounds similar to this one have been studied for their biological activities, making them interesting candidates for drug development. The structural components can influence *pharmacological properties* significantly.
Synthesis Challenges: Creating this compound demands a good grasp of both synthetic methodologies and the reactivity of the constituent parts. The introduction of the ethoxycarbonyl group adds a layer of complexity in synthetic routes.
Interdisciplinary Interest: This compound not only piques the interest of synthetic chemists but also draws the attention of researchers in fields like medicinal chemistry, materials science, and environmental chemistry.

As scientists continue to explore the potential applications of N-(3-chloro-4-iodo-phenyl)-1-ethoxycarbonylsulfanyl-methanimidothioic acid, it stands out as an exciting topic of study in the broader landscape of chemical innovation. Its unique characteristics and possible applications open doors to *new discoveries and advancements* in multiple scientific realms.