1-allylsulfanyl-N-(1-phenylethyl)methanimidothioic acid

Identification

Molecular formula

C₁₂H₁₅NS₂

IUPAC name

State

At room temperature, 1-allylsulfanyl-N-(1-phenylethyl)methanimidothioic acid is usually in a liquid state.

Melting point (Celsius)

78.00

Melting point (Kelvin)

351.15

Boiling point (Celsius)

239.00

Boiling point (Kelvin)

512.15

General information

Molecular weight

224.35g/mol

Molar mass

224.3520g/mol

Density

1.1200g/cm³

Appearence

The compound is generally a colorless to pale yellow liquid, possessing a slight phenolic or sulfurous odor. It may exhibit a viscous consistency depending on its precise purity and mode of preparation.

Comment on solubility

Solubility Overview

The compound 1-allylsulfanyl-N-(1-phenylethyl)methanimidothioic acid demonstrates intriguing solubility characteristics that are essential for its potential applications in various chemical contexts.

Factors Influencing Solubility

The solubility of this compound can be influenced by several key factors:

Polarity: Due to the presence of both polar and non-polar functional groups, the overall polarity of the molecule can lead to variable solubility in different solvents.
Temperature: As with many organic compounds, increasing the temperature often enhances solubility, allowing for better solvation of the molecule.
pH of the solution: The acidic nature of the thiol-thioic acid group may affect solubility in aqueous solutions, particularly in various pH environments.
Solvent Interaction: In polar solvents (e.g., water, ethanol), the compound may show different solubility profiles compared to non-polar solvents (e.g., hexane, toluene).

Predicted Solubility Behavior

In general, one might expect that:

In polar solvents, the interaction with the functional groups could lead to moderate solubility.
In non-polar solvents, the solubility may decrease due to poor interaction with the solvent.

Overall, the solubility of 1-allylsulfanyl-N-(1-phenylethyl)methanimidothioic acid is likely a combination of its unique molecular structure and the environmental conditions in which it is placed. Understanding these solubility dynamics is crucial for its utilization in practical applications.

Interesting facts

Interesting Facts about 1-Allylsulfanyl-N-(1-phenylethyl)methanimidothioic Acid

This intriguing compound is a part of the family of thioamides, a subset of compounds known for their pivotal roles in both organic synthesis and medicinal chemistry. 1-Allylsulfanyl-N-(1-phenylethyl)methanimidothioic acid not only showcases unique structure but also acts as a significant building block in the development of various pharmaceuticals due to its biological activity.

Key Features and Applications

Thioamide Functionality: The presence of both sulfur and nitrogen functionalities positions this compound as an interesting candidate for coordinating with metallic catalysts.
Biological Activity: Thioamides, including this compound, are often studied for their potential as antibacterial or antifungal agents, making them essential in pharmaceutical research.
Potential Reactivity: The allyl group introduces possibilities for diverse reactivity patterns, enabling facile transformations under various conditions.
Interdisciplinary Importance: This compound finds relevance not just in organic chemistry, but also in medicinal chemistry and materials science.

Furthermore, studying such complex compounds aids in understanding intricate chemical reactions and mechanisms. As highlighted by renowned chemist Derek Lowe, "The simplest compounds often lead to the most groundbreaking discoveries." This particular compound exemplifies how intricate variations in structure can lead to valuable chemical diversity.

Overall, 1-Allylsulfanyl-N-(1-phenylethyl)methanimidothioic acid is a fine example of how specific functionalizations can give rise to versatile compounds that are ripe for scientific exploration and technological innovation.