N-(3,4-dichlorophenyl)-1-methylsulfanyl-methanimidothioic acid

Identification

Molecular formula

C₈H₆Cl₂NS₃

CAS number

99129-21-2

IUPAC name

N-(3,4-dichlorophenyl)-1-methylsulfanyl-methanimidothioic acid

State

At room temperature, N-(3,4-dichlorophenyl)-1-methylsulfanyl-methanimidothioic acid exists as a solid. It does not sublimate or significantly evaporate at standard temperature and pressure conditions.

Melting point (Celsius)

157.00

Melting point (Kelvin)

430.15

Boiling point (Celsius)

413.20

Boiling point (Kelvin)

686.35

General information

Molecular weight

288.18g/mol

Molar mass

288.1800g/mol

Density

1.6480g/cm³

Appearence

The compound is typically a yellow solid. Its crystalline form is often used in a laboratory setting. The intensity of the yellow color may vary slightly depending on purity and specific preparation methods.

Comment on solubility

Solubility of N-(3,4-dichlorophenyl)-1-methylsulfanyl-methanimidothioic acid

The solubility of N-(3,4-dichlorophenyl)-1-methylsulfanyl-methanimidothioic acid (C₈H₆Cl₂NS₃) can be quite intriguing due to its unique structural components. Here are some important points regarding its solubility:

Polarity: Given the presence of chlorine atoms and sulfur groups, this compound may exhibit varying degrees of polarity, impacting its solubility in different solvents.
Solvent Interaction: It is likely to be more soluble in organic solvents (like acetone or dimethyl sulfoxide) compared to polar solvents (like water) due to the hydrophobic character imparted by its aromatic rings.
pH Dependence: The carboxylic acid functionality suggests that the solubility might also depend significantly on the pH of the solution. In acidic conditions, the compound may remain in its undissociated form, while in more basic conditions, anionic forms could enhance solubility.
Temperature Influence: As with many compounds, varying the temperature can affect solubility; generally, increased temperature can lead to higher solubility in organic solvents.

In summary, the solubility profile of N-(3,4-dichlorophenyl)-1-methylsulfanyl-methanimidothioic acid is shaped by its polarity, solvent choice, pH, and temperature—characteristics that make it an interesting subject for further study in chemical behavior.

Interesting facts

Interesting Facts About N-(3,4-Dichlorophenyl)-1-methylsulfanyl-methanimidothioic Acid

N-(3,4-dichlorophenyl)-1-methylsulfanyl-methanimidothioic acid is a fascinating chemical compound that plays a crucial role in various scientific applications. Here are some noteworthy aspects of this compound:

Synthesis and Structure: This compound features a unique ^{3,4-dichlorophenyl} moiety, contributing to its chemical reactivity and potential biological properties. The presence of sulfur in its structure adds to its unique characteristics.
Biological Significance: Compounds with similar structures are often studied for their potential antimicrobial and antifungal properties. Researchers are keenly investigating their mechanisms to improve drug development processes.
Environmental Relevance: The chlorophenyl group is of particular interest in studies on environmental contaminants. Understanding how such compounds behave in ecological systems can aid in assessing their impact.
Analytical Techniques: The analysis of this compound often requires advanced techniques. Methods such as High-Performance Liquid Chromatography (HPLC) and Nuclear Magnetic Resonance (NMR) spectroscopy can effectively characterize its features.

In summary, while not as widely recognized as some other chemical compounds, N-(3,4-dichlorophenyl)-1-methylsulfanyl-methanimidothioic acid offers intriguing opportunities for research in various fields, from medicinal chemistry to environmental science. As one researcher wisely said, “Chemistry is the study of transformation, and each compound tells its own compelling story.”