N-(4-chloro-3-methylphenyl)-1-methylsulfanyl-methanimidothioic acid

Identification

Molecular formula

C₁₀H₁₂ClNOS₂

CAS number

327-59-9

IUPAC name

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

State

This compound is usually a crystalline solid at room temperature. It is stable under normal temperature and pressure conditions when stored appropriately.

Melting point (Celsius)

117.40

Melting point (Kelvin)

390.55

Boiling point (Celsius)

332.40

Boiling point (Kelvin)

605.55

General information

Molecular weight

289.84g/mol

Molar mass

289.8400g/mol

Density

1.3000g/cm³

Appearence

N-(4-chloro-3-methylphenyl)-1-methylsulfanyl-methanimidothioic acid is generally found as a crystalline solid. The color can range from white to pale yellow, depending on the purity and specific crystalline form.

Comment on solubility

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

N-(4-chloro-3-methyl-phenyl)-1-methylsulfanyl-methanimidothioic acid is an intriguing compound with unique solubility characteristics that can influence its application in various fields. When considering solubility, various factors come into play:

Polarity: This compound exhibits polar functional groups which generally enhance solubility in polar solvents such as water.
Hydrogen bonds: The presence of functional groups capable of forming hydrogen bonds can lead to improved solubility in protic solvents.
Solvent compatibility: It is crucial to evaluate the solubility in organic solvents (like methanol or ethanol) versus aqueous solutions, as the structure suggests variable solubility depending on the solvent choice.
Temperature dependence: The solubility may vary significantly with temperature; typically, increasing temperature enhances solubility for many compounds.

In conclusion, while the specific solubility data for N-(4-chloro-3-methyl-phenyl)-1-methylsulfanyl-methanimidothioic acid might be limited, its structural characteristics provide valuable insights into its potential solubility behavior. Experimentation is essential to uncover the precise solubility profile, leading to a deeper understanding and potential applications of this compound.

Interesting facts

Interesting Facts About N-(4-chloro-3-methyl-phenyl)-1-methylsulfanyl-methanimidothioic acid

N-(4-chloro-3-methyl-phenyl)-1-methylsulfanyl-methanimidothioic acid, often referred to for its biological importance, is a captivating compound with several noteworthy aspects. Below are some intriguing facts that highlight its significance in the field of chemistry:

Biological Relevance: This compound has gained attention for its potential role in pharmacology. Its structure suggests that it may interact with biological systems, possibly acting as an inhibitor or modulator of specific biological pathways.
Thiocarbamates Origins: The presence of the thiocarbonyl group in its structure indicates that it belongs to a class of compounds known as thiocarbamates, which are known for their diverse biological activity, including anti-inflammatory and anticancer properties.
Synthetic Applications: Chemists have leveraged compounds like this one in synthetic organic chemistry to create more complex molecules, which can be beneficial in drug discovery and development.
Environmental Considerations: Understanding the behavior of this compound in various environmental conditions is crucial. Compounds with sulfur and chlorine atoms can exhibit unique reactivity, which can impact ecological systems.
Research Potential: Ongoing research seeks to uncover new applications and mechanisms of action for similar structures. The study of such compounds may lead to the development of novel therapeutic agents.

As a final thought, the complexity of N-(4-chloro-3-methyl-phenyl)-1-methylsulfanyl-methanimidothioic acid's structure stands as a testament to the intricate interplay of chemistry and biology. As scientists delve deeper into its properties, they may unveil further surprises that enhance our understanding of chemical interactions and their implications.