N-(4-iodo-3-methylphenyl)-1-methylthioformamidothioic acid

Identification

Molecular formula

C₁₀H₁₂IN₂OS₂

CAS number

27414-87-7

IUPAC name

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

State

At room temperature, this compound is a solid. The iodine atom contributes to its relatively high molecular weight, and the sulfanyl group can influence its stability in various environments.

Melting point (Celsius)

167.80

Melting point (Kelvin)

440.90

Boiling point (Celsius)

324.30

Boiling point (Kelvin)

597.50

General information

Molecular weight

341.21g/mol

Molar mass

341.2120g/mol

Density

1.9723g/cm³

Appearence

The compound typically appears as a solid with a crystalline structure. The presence of iodine often imparts a distinct color that ranges from colorless to slightly yellow, though the specific appearance can vary based on purity and form.

Comment on solubility

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

The solubility of chemical compounds is a complex topic influenced by various factors, including molecular structure, polarity, and temperature. For the compound N-(4-iodo-3-methyl-phenyl)-1-methylsulfanyl-methanimidothioic acid, solubility can be considered with the following points in mind:

Polar and Nonpolar Interactions: The presence of both polar (due to the sulfenyl group) and nonpolar (due to the aromatic rings) elements in the structure may lead to limited solubility in water, as these opposing characteristics can hinder dissolution.
Solvent Compatibility: This compound might be more soluble in organic solvents, such as ethanol or dichloromethane, which can effectively interact with its structure's nonpolar parts.
Hydrogen Bonding Potential: The potential for hydrogen bonding in this compound, particularly due to the thiourea-like functional groups, could allow for some solubility in polar solvents, albeit likely not very high.
Temperature Dependence: As with many compounds, solubility may increase with temperature, enabling better dissolution in specific solvents.

In summary, while the exact solubility profile of N-(4-iodo-3-methyl-phenyl)-1-methylsulfanyl-methanimidothioic acid requires experimental determination, understanding its structural components provides useful insights into its likely behavior in different solvent environments.

Interesting facts

Interesting Facts about N-(4-Iodo-3-methyl-phenyl)-1-methylsulfanyl-methanimidothioic Acid

N-(4-iodo-3-methyl-phenyl)-1-methylsulfanyl-methanimidothioic acid is a fascinating compound that showcases the intricacies of organosulfur chemistry. It exemplifies how simple modifications can significantly alter the properties and potential applications of a chemical compound. Here are some intriguing points about this compound:

Structural Diversity: The presence of an iodine atom in its structure contributes to the compound's unique reactivity, often allowing for engaging substitution reactions.
Biological Relevance: Compounds like this are frequently explored for their potential biological activities, including antimicrobial and antitumor properties, making them valuable in pharmaceutical research.
Synthesis Pathways: Chemists often use various synthetic strategies to evoke functionality in similar compounds, thereby expanding their utility in organic synthesis.
Potential Applications: The thioamide functional group in this compound is known for its role in agricultural chemicals, hinting at possible use cases in agrochemistry.
Nanotechnology Connections: Recent studies have indicated that such compounds could also play a role in the development of nanomaterials or catalysts.

In the words of a renowned chemist, "The beauty of chemistry lies in its ability to combine seemingly simple elements into a tapestry of complex interactions and products." This compound is a case in point, illustrating how changing just a few components can yield a substance with remarkable properties and potential applications.

In summary, N-(4-iodo-3-methyl-phenyl)-1-methylsulfanyl-methanimidothioic acid is not only an exploration of chemical structure but also a gateway into understanding the rich applications and possibilities that modern chemistry offers.