1-ethylsulfanyl-N-phenyl-methanimidothioic acid

Identification

Molecular formula

C₁₀H₁₃NS₂

CAS number

Unknown

IUPAC name

1-ethylsulfanyl-N-phenyl-methanimidothioic acid

State

At room temperature, 1-ethylsulfanyl-N-phenyl-methanimidothioic acid is typically in a solid state. Its aromatic ring and sulfanyl groups contribute to its solid crystal formation due to intermolecular interactions.

Melting point (Celsius)

102.00

Melting point (Kelvin)

375.00

Boiling point (Celsius)

281.00

Boiling point (Kelvin)

554.00

General information

Molecular weight

227.36g/mol

Molar mass

227.3550g/mol

Density

1.2600g/cm³

Appearence

This compound typically appears as a yellowish crystalline solid. The crystalline nature is indicative of its organised molecular structure, which is common among compounds with aromatic groups or extensive conjugation, such as the phenyl group present in the structure.

Comment on solubility

Solubility of 1-ethylsulfanyl-N-phenyl-methanimidothioic acid

The solubility of 1-ethylsulfanyl-N-phenyl-methanimidothioic acid is an intriguing area of study due to its unique chemical structure. This compound possesses both polar and non-polar functional groups, which influences its solubility in various solvents.

Solubility Characteristics:

Polarity: The presence of the thioic acid group contributes to polar characteristics, suggesting solubility in polar solvents like water.
Hydrophobicity: The ethylsulfanyl and phenyl groups add hydrophobic properties, indicating potential solubility in organic solvents such as ethanol or acetone.
Solvent Interaction: The ability to form hydrogen bonds with solvents is essential in determining the overall solubility.

In general, 1-ethylsulfanyl-N-phenyl-methanimidothioic acid is likely to exhibit variable solubility, depending on the solvent used. For practical applications, it is suggested to consider both polar and non-polar solvents when investigating the solubility of this complex compound.

This multifaceted solubility behavior makes it a fascinating subject for further research, as understanding solubility can greatly influence its application in various chemical processes.

Interesting facts

Interesting Facts about 1-Ethylsulfanyl-N-phenyl-methanimidothioic Acid

1-Ethylsulfanyl-N-phenyl-methanimidothioic acid is a compound that showcases the fascinating interplay of organic chemistry and biological activity. Here are some intriguing aspects of this compound:

Unique Structure: This compound features a thioic acid group, which is notable for its sulfur atom. Sulfur-containing compounds are often involved in a variety of reactions and have distinct chemical properties compared to their oxygen counterparts.
Potential Biological Activity: Research has suggested that compounds with thioic acid moieties may exhibit antimicrobial and antifungal properties, indicating possible applications in pharmacology and medicinal chemistry.
Synergistic Effects: The ethylsulfanyl and phenyl groups in the structure may work together synergistically, enhancing the biological activity of the compound—a relationship that chemists find particularly interesting.
Versatile Chemistry: This compound can undergo various chemical transformations, making it a valuable building block in organic synthesis. It can be used to create derivatives with a wide range of applications.
Environmental Considerations: Understanding the behavior of such compounds in the environment can provide insights into their stability and breakdown, which is essential for assessing their ecological impact.

In summary, 1-ethylsulfanyl-N-phenyl-methanimidothioic acid is a compound that—through its structure and potential applications—highlights the intricate and rich landscape of organic chemistry. As scientists continue to explore its properties, we may uncover even more intriguing uses for this compound.