1-methylsulfanyl-N-(3-nitrophenyl)methanimidothioic acid

Identification

Molecular formula

C₈H₈N₂O₂S₂

CAS number

68892-67-3

IUPAC name

1-methylsulfanyl-N-(3-nitrophenyl)methanimidothioic acid

State

At room temperature, this compound is typically a solid. It can be handled in powdered form, and proper safety measures should be taken to avoid inhalation or contact with the skin.

Melting point (Celsius)

177.00

Melting point (Kelvin)

450.15

Boiling point (Celsius)

405.00

Boiling point (Kelvin)

678.15

General information

Molecular weight

245.32g/mol

Molar mass

245.3170g/mol

Density

1.3780g/cm³

Appearence

The compound typically appears as a yellow solid, often crystalline in nature. It may exhibit a powdery texture, depending on its form and purity. The color can vary slightly based on specific conditions and purity levels.

Comment on solubility

Solubility of 1-methylsulfanyl-N-(3-nitrophenyl)methanimidothioic acid

The solubility of 1-methylsulfanyl-N-(3-nitrophenyl)methanimidothioic acid can be influenced by various factors, including temperature, pH, and the solvent used. While specific data on this compound might be limited, we can consider some general traits that typically govern its solubility:

Polarity: Compounds with significant polar functional groups tend to exhibit higher solubility in polar solvents (such as water) compared to non-polar solvents.
Hydrogen Bonding: The ability to form hydrogen bonds can enhance solubility in aqueous environments.
Structural Characteristics: The presence of methyl and nitro groups can affect the overall chemical interactions, impacting the solubility.

According to the principle of "like dissolves like," one could hypothesize that this compound might show limited solubility in water but could be better dissolved in organic solvents. It is essential to conduct experimental solubility tests to obtain accurate data, as theoretical predictions can vary significantly depending on the local environment and intermolecular forces involved.

In summary, while the solubility of 1-methylsulfanyl-N-(3-nitrophenyl)methanimidothioic acid warrants further investigation, understanding the factors outlined above provides a foundational perspective on how its solubility might behave.

Interesting facts

Interesting Facts about 1-Methylsulfanyl-N-(3-nitrophenyl)methanimidothioic Acid

This intriguing compound is a great example of how modifications in molecular structure can lead to unique chemical properties and potential applications. Here are some notable aspects:

Functional Diversity: The presence of both methyl sulfanyl and nitrophenyl groups enhances the compound's reactivity, making it a valuable candidate in organic synthesis and pharmaceuticals.
Bioactivity: Compounds like 1-methylsulfanyl-N-(3-nitrophenyl)methanimidothioic acid may exhibit biological activities, which could be useful in developing new medicines, especially in targeting specific pathways in various diseases.
Structure-Activity Relationship: The incorporation of the nitro group is significant, as it's known to affect electron distribution, potentially influencing the compound’s mechanism of action in biological systems.
Research Relevance: With the increasing interest in thioic acids and their derivatives, this compound is a noteworthy subject within the field of medicinal chemistry, particularly for its potential in drug discovery.

One of the fascinating aspects of studying compounds like this is their potential role in the development of innovative therapies. As emphasized by researchers, "Exploring the chemical diversity allows us to unlock new pathways toward enhanced drug efficacy." Furthermore, understanding the behavior of such compounds in various environments can provide insight into their stability and effectiveness as therapeutic agents.

In summary, 1-methylsulfanyl-N-(3-nitrophenyl)methanimidothioic acid stands out due to its intriguing structure and potential applications, exemplifying the intricate relationship between chemical composition and biological activity.