N-(4-bromophenyl)-1-methylsulfanyl-methanimidothioic acid

Identification

Molecular formula

C₉H₉BrNOS₂

CAS number

35612-24-1

IUPAC name

N-(4-bromophenyl)-1-methylsulfanyl-methanimidothioic acid

State

At room temperature, it is typically found in a solid state, characterized by its crystalline nature. It remains stable under normal conditions of use and storage.

Melting point (Celsius)

83.20

Melting point (Kelvin)

356.35

Boiling point (Celsius)

230.40

Boiling point (Kelvin)

503.55

General information

Molecular weight

278.18g/mol

Molar mass

278.1840g/mol

Density

1.6700g/cm³

Appearence

The compound typically appears as a crystalline solid, characterized by its colorless to pale yellow appearance. The crystals are usually well-formed and have a slight sheen due to their crystalline nature.

Comment on solubility

Solubility of N-(4-bromophenyl)-1-methylsulfanyl-methanimidothioic acid

N-(4-bromophenyl)-1-methylsulfanyl-methanimidothioic acid, like many organic compounds, exhibits unique solubility characteristics that can greatly influence its behavior in various chemical environments. Understanding its solubility is essential for applications in both synthetic chemistry and biological systems.

Key Points on Solubility:

Polarity: The presence of polar functional groups in its structure can lead to potential hydrophilic interactions, allowing for some degree of solubility in polar solvents.
Solvent Compatibility: This compound may be more soluble in organic solvents such as dimethyl sulfoxide (DMSO) and ethanol, while showing limited solubility in water due to the bulky bromine substituent which hinders its ability to interact with solvent molecules.
Temperature Influence: The solubility can also be affected by temperature; typically, increased temperature enhances the solubility of most organic compounds.
pH Dependence: Being a carboxylic acid derivative, its solubility might vary significantly with changes in pH, especially in aqueous solutions.

In conclusion, while N-(4-bromophenyl)-1-methylsulfanyl-methanimidothioic acid may not be highly soluble in water, its solubility profiles in various organic solvents and under changing conditions are crucial for its utilization in chemical processes. As with many compounds, practical experimentation is often required to determine the most effective solvent for desired applications.

Interesting facts

Interesting Facts about N-(4-bromophenyl)-1-methylsulfanyl-methanimidothioic acid

N-(4-bromophenyl)-1-methylsulfanyl-methanimidothioic acid is a fascinating compound that showcases the intricate world of organic chemistry. Here are some intriguing aspects of this compound:

Structural Complexity: This compound features a unique combination of functional groups, including a bromophenyl moiety and a methylsulfanyl group, making it an interesting subject of study for chemists interested in developing complex synthesis pathways.
Potential Applications: Given the presence of the bromine atom, compounds like this often exhibit biological activity. They may serve as intermediates in pharmaceuticals or agrochemicals, highlighting the importance of methodical research in medicinal chemistry.
Reactivity Insights: The thioic acid component may contribute to interesting reactivity patterns, particularly in nucleophilic substitution reactions or in the formation of stable complexes with metal ions.
Environmental Impact: Studying compounds containing bromine and sulfur can provide insights into their environmental behavior and health effects, making it relevant for those working in environmental chemistry or toxicology.
Chemical Characterization: N-(4-bromophenyl)-1-methylsulfanyl-methanimidothioic acid serves as an ideal candidate for advanced characterization techniques such as NMR spectroscopy and mass spectrometry, enabling chemists to delve deep into its molecular structure.
Research Opportunities: Researchers continue to explore the reactivity and applications of similar compounds, focusing on developing novel derivatives that could lead to innovative solutions in various fields.

In conclusion, N-(4-bromophenyl)-1-methylsulfanyl-methanimidothioic acid is more than just a molecular structure; it represents a bridge to deeper understanding in chemistry, promising opportunities for discovery and application.