N-(4-chloro-3-methyl-phenyl)-1-ethylsulfanyl-methanimidothioic acid

Identification

Molecular formula

C₁₀H₁₂ClNS₂

CAS number

IUPAC name

N-(4-chloro-3-methyl-phenyl)-1-ethylsulfanyl-methanimidothioic acid

State

At room temperature, the compound is in a solid state.

Melting point (Celsius)

62.00

Melting point (Kelvin)

335.15

Boiling point (Celsius)

394.00

Boiling point (Kelvin)

667.15

General information

Molecular weight

257.79g/mol

Molar mass

257.7900g/mol

Density

1.2600g/cm³

Appearence

N-(4-chloro-3-methyl-phenyl)-1-ethylsulfanyl-methanimidothioic acid typically appears as a crystalline solid. The exact color may vary depending on purity, but it can often be found in a pale yellow to off-white hue.

Comment on solubility

Solubility of N-(4-chloro-3-methyl-phenyl)-1-ethylsulfanyl-methanimidothioic acid

N-(4-chloro-3-methyl-phenyl)-1-ethylsulfanyl-methanimidothioic acid, with its complex structure, exhibits unique solubility characteristics that are primarily influenced by its functional groups. The solubility of such compounds can vary significantly depending on the solvent used.

Key points regarding the solubility of this compound include:

Polarity: The presence of polar thioic acid groups generally enhances solubility in polar solvents like water.
Hydrogen Bonding: The acid group may form hydrogen bonds with water molecules, increasing its solubility in aqueous environments.
Non-polar Characteristics: The aromatic and alkyl groups contribute to a hydrophobic character, which can limit solubility in strictly polar solvents.
Solvent Selection: This compound might be more soluble in organic solvents (e.g., ethanol, acetone) due to the interactions with its non-polar regions.

As a general trend, one might find that:

Solubility increases with rising temperature for polar solvents.
Solubility can decrease in highly polar environments if overshadowed by non-polar characteristics.

Ultimately, experimentation is key to determining the precise solubility profile of N-(4-chloro-3-methyl-phenyl)-1-ethylsulfanyl-methanimidothioic acid in various solvents.

Interesting facts

Interesting Facts about N-(4-chloro-3-methyl-phenyl)-1-ethylsulfanyl-methanimidothioic acid

N-(4-chloro-3-methyl-phenyl)-1-ethylsulfanyl-methanimidothioic acid is a fascinating compound that showcases the diversity and complexity of organic sulfur chemistry. Here are some notable aspects of this compound:

Sulfur Incorporation: The inclusion of sulfur in its structure is a significant feature. Sulfur-containing compounds often exhibit unique properties and reactivity profiles, making them valuable in various chemical applications, particularly in the creation of agrochemicals and pharmaceuticals.
Chlorine Modification: The presence of chlorine (Cl) in the aromatic ring increases the compound's versatility by influencing its electronic properties. Such halogens can enhance biological activity and modify molecular interactions, which is crucial for drug design.
Molecular Configuration: This compound's structure highlights the concept of chirality, where different spatial arrangements can lead to varied biological outcomes. Understanding chirality is essential in medicinal chemistry to maximize efficacy and minimize side effects.
Biological Relevance: The structure suggests potential applications in agriculture as a pesticide or herbicide. These sulfur thio acids often exhibit plant protection qualities, playing a vital role in sustainable agriculture.
Research Potential: Continuous studies on compounds like this one can lead to innovations in materials science, particularly in developing new coatings, antioxidants, or other functional materials.

This compound exemplifies how even minor alterations in chemical structure can lead to significant changes in functionality and application, underscoring the importance of detailed molecular analysis in the field of chemistry.

In the words of renowned chemist Linus Pauling, "The best way to have a good idea is to have a lot of ideas." Exploring such complex compounds expands the boundaries of our understanding and opens new avenues in research.