N-(3-chlorophenyl)-1-ethylsulfanyl-methanimidothioic acid

Identification

Molecular formula

C₁₀H₁₁ClNOS₂

CAS number

87318-52-7

IUPAC name

N-(3-chlorophenyl)-1-ethylsulfanyl-methanimidothioic acid

State

At room temperature, the compound is generally found as a solid. It maintains stability in this form under standard conditions.

Melting point (Celsius)

125.00

Melting point (Kelvin)

398.15

Boiling point (Celsius)

295.00

Boiling point (Kelvin)

568.15

General information

Molecular weight

255.78g/mol

Molar mass

255.7780g/mol

Density

1.3450g/cm³

Appearence

The compound is typically a crystalline solid. Its color can range from white to a light yellow depending on its purity level. Being a sulfur-containing compound, it may have a distinct odor.

Comment on solubility

Solubility of N-(3-chlorophenyl)-1-ethylsulfanyl-methanimidothioic acid

The solubility of N-(3-chlorophenyl)-1-ethylsulfanyl-methanimidothioic acid is influenced by several factors, primarily its chemical structure and environmental conditions. Understanding its solubility can help in various applications, particularly in pharmaceuticals and agrochemicals. Here are some key points regarding its solubility:

Polarity: The presence of polar functional groups in its structure may enhance solubility in polar solvents.
Solvent Effects: This compound may exhibit varying solubility in water compared to organic solvents. It is likely to be more soluble in organic solvents due to its hydrophobic characteristics.
Temperature Influence: Increased temperature may increase solubility, a common trend observed with many chemical compounds.
pH Sensitivity: Solubility may also vary with changes in pH, especially if it can exist in protonated or deprotonated forms.

In summary, the solubility characteristics of N-(3-chlorophenyl)-1-ethylsulfanyl-methanimidothioic acid can be complex due to its unique structure. *Understanding these properties is essential* for its practical applications and effective utilization in various fields.

Interesting facts

Interesting Facts about N-(3-Chlorophenyl)-1-Ethylsulfanyl-Methanimidothioic Acid

N-(3-Chlorophenyl)-1-ethylsulfanyl-methanimidothioic acid, while its name may seem complex, offers a fascinating glimpse into the world of thioamides, a subclass of compounds that have garnered significant attention in the field of organic chemistry. Here are some compelling facts:

Thioamide Properties: This compound belongs to the thioamide family, which is known for having a sulfur atom replacing the oxygen atom found in amides. This substitution often leads to unique reactivity patterns and different chemical properties.
Pharmaceutical Applications: Compounds like this one are often studied for their potential in medicinal chemistry. Their unique functional groups can lead to the development of new drugs that target various biological pathways.
Role of Chlorine: The presence of the 3-chlorophenyl group is particularly interesting. Chlorine atoms can significantly influence the compound's biological activity and how it interacts with other molecules, making it a point of interest in synthesis and pharmacology.
Environmental Considerations: Some thioamides have been investigated for their environmental impact and potential use in herbicides and pesticides. Understanding their chemical behavior helps in assessing safety and efficacy in agricultural applications.
Research Opportunities: This compound showcases the interplay between structure and function, offering opportunities for research in synthesis methods, reactivity, and application in various fields from biotechnology to materials science.

As we delve into the intricate designs of chemical compounds like N-(3-chlorophenyl)-1-ethylsulfanyl-methanimidothioic acid, it becomes evident that the world of chemistry is a blend of creativity and science. Just as chemist Linus Pauling once said, "The best way to have a good idea is to have a lot of ideas". This compound represents one of many intriguing ideas waiting to be explored!