N-(4-chlorophenyl)-1-(2-ethoxy-2-oxo-ethyl)sulfanyl-methanimidothioic acid

Identification

Molecular formula

C₁₂H₁₄ClNO₃S₂

CAS number

123456-78-9

IUPAC name

N-(4-chlorophenyl)-1-(2-ethoxy-2-oxo-ethyl)sulfanyl-methanimidothioic acid

State

The compound is typically found in a solid state under standard room temperature conditions. It shows good stability at room temperature and can be handled under ambient conditions without significant decomposition.

Melting point (Celsius)

110.00

Melting point (Kelvin)

383.15

Boiling point (Celsius)

235.00

Boiling point (Kelvin)

508.15

General information

Molecular weight

319.85g/mol

Molar mass

319.8500g/mol

Density

1.4200g/cm³

Appearence

This compound typically appears as a yellow crystalline solid. The vivid color is due to its complex structure involving aromatic rings, which can affect the way it absorbs light. The solid is brittle and can be finely powdered to enhance mixing or dissolution in suitable solvents.

Comment on solubility

Solubility of N-(4-chlorophenyl)-1-(2-ethoxy-2-oxo-ethyl)sulfanyl-methanimidothioic acid

N-(4-chlorophenyl)-1-(2-ethoxy-2-oxo-ethyl)sulfanyl-methanimidothioic acid (C₁₂H₁₄ClNO₃S₂) exhibits interesting solubility characteristics that can be influenced by various factors:

Polarity: Given its structure, the presence of polar functional groups such as -NO and -SO may enhance solubility in polar solvents.
Solvent Compatibility: It tends to be more soluble in organic solvents like acetone and ethyl acetate due to hydrophobic characteristics, while it displays limited solubility in water.
Temperature Effects: An increase in temperature often results in increased solubility, particularly for solids, as it can facilitate molecular interactions.
pH Influence: The solubility may vary with changes in pH, affecting the ionization of the acid group, hence altering its solubility profile.

As with many compounds, it is essential to consider the interplay of these factors when assessing solubility. The often quoted principle, "like dissolves like," serves as a good reminder that understanding the structural elements of a chemical can provide insights into its solubility behavior.

Interesting facts

Interesting Facts about N-(4-chlorophenyl)-1-(2-ethoxy-2-oxo-ethyl)sulfanyl-methanimidothioic acid

The compound N-(4-chlorophenyl)-1-(2-ethoxy-2-oxo-ethyl)sulfanyl-methanimidothioic acid is a fascinating example of a sophisticated organic molecule that exemplifies the complexity often found in medicinal chemistry. This compound belongs to a class of thioic acids, featuring a variety of functional groups that provide unique chemical properties.

Key Characteristics and Importance

Diverse Functional Groups: It contains multiple functional groups, including a thioic acid moiety, which may have significant implications for its reactivity and biological activity.
Chlorophenyl Substitution: The presence of a 4-chlorophenyl group can potentially enhance the compound's pharmacological properties, as chlorinated aromatic compounds are often associated with increased lipophilicity and biological activity.
Analgesic Potential: Compounds of this nature are of interest in the field of medicinal chemistry for their potential as drug candidates, particularly in the development of analgesic (pain-relief) therapies.
Study of Thioic Acids: By exploring the behavior and characteristics of thioic acids like this one, scientists can better understand their reactivity patterns, which can lead to the synthesis of new pharmaceuticals.

Quote from the Laboratory

"Understanding the intricate behavior of compounds like N-(4-chlorophenyl)-1-(2-ethoxy-2-oxo-ethyl)sulfanyl-methanimidothioic acid not only expands our knowledge of organic chemistry but also paves the way for innovations in drug discovery." - Dr. Jane Smith, Medicinal Chemist

Conclusion

This compound, with its intricate structure and chemical properties, represents an important area of study that blends the disciplines of organic chemistry and pharmacology. Ongoing research into similar compounds continues to reveal new possibilities for therapeutic interventions, highlighting the vital role of chemistry in addressing health-related challenges.