1-Allylsulfanyl-N-(4-chlorophenyl)methanimidothioic acid

Identification

Molecular formula

C₁₀H₁₀ClNO₁S₂

CAS number

148529-74-8

IUPAC name

1-allylsulfanyl-N-(4-chlorophenyl)methanimidothioic acid

State

At room temperature, 1-Allylsulfanyl-N-(4-chlorophenyl)methanimidothioic acid is a solid.

Melting point (Celsius)

132.00

Melting point (Kelvin)

405.15

Boiling point (Celsius)

356.00

Boiling point (Kelvin)

629.15

General information

Molecular weight

243.75g/mol

Molar mass

243.7500g/mol

Density

1.4000g/cm³

Appearence

The compound appears as a crystalline solid with a pale yellow color. It typically exhibits a characteristic odor associated with organic sulfur compounds.

Comment on solubility

Solubility of 1-allylsulfanyl-N-(4-chlorophenyl)methanimidothioic acid

The solubility of 1-allylsulfanyl-N-(4-chlorophenyl)methanimidothioic acid in various solvents provides insight into its chemical behavior and potential applications. This compound is generally characterized by its unique structure, which can influence its interaction with solvents.

When examining its solubility, it is important to consider the following key points:

Polar vs. Non-Polar Solvents: The presence of both polar (such as the -NH group) and non-polar groups (such as the allyl and phenyl functionalities) suggests that 1-allylsulfanyl-N-(4-chlorophenyl)methanimidothioic acid may be soluble in a variety of solvents. It is likely to be more soluble in polar protic solvents due to hydrogen bonding capabilities.
Temperature Influence: Solubility tends to increase with temperature for many organic compounds. Thus, examining this compound's solubility at different temperatures may yield interesting results.
pH Dependence: As a thiol acid derivative, its solubility may also be affected by the pH of the solution, which can influence the ionization state of the molecule.
Experimental Determination: For precise applications, experimental solubility data in specific solvents is essential to understand practical uses in synthesis and formulation.

In conclusion, while 1-allylsulfanyl-N-(4-chlorophenyl)methanimidothioic acid exhibits soluble characteristics, the precise conditions must be explored to determine optimal solubility parameters. Detailing these interactions further can expand its potential applications in various chemical processes.

Interesting facts

Interesting Facts about 1-Allylsulfanyl-N-(4-chlorophenyl)methanimidothioic Acid

This intriguing compound belongs to the class of thioimidates, which are essential in various chemical processes and applications. As a researcher or a chemistry enthusiast, you might find the following points about this compound particularly fascinating:

Structure and Functionality: The presence of both an allyl group and a chlorophenyl moiety provides unique reactivity patterns. The functional groups can engage in multiple chemical reactions, thus serving as effective intermediates in organic synthesis.
Biological Significance: Compounds like 1-allylsulfanyl-N-(4-chlorophenyl)methanimidothioic acid have drawn attention due to their potential pharmacological properties. The thioic acid component may exhibit interesting biological activity, which warrants further investigation.
Applications in Synthesis: This compound could play a pivotal role in synthesizing other complex molecules, potentially including pharmaceuticals and agrochemicals. Its reactivity could be explored in various synthetic pathways.
Research Opportunities: The intriguing structure poses numerous opportunities for studying reaction mechanisms, which can enhance our understanding of chemical behavior under different conditions.

As one delves deeper into the world of such compounds, one can’t help but appreciate the rich tapestry of chemical interactions at play. "The beauty of chemistry lies in its complexity, where every compound tells a story of its atoms and bonds." This particular compound is an excellent example of how even seemingly simple structures can lead to significant discoveries and applications in science.