N-(3-chlorophenyl)-1-[(4-chlorophenyl)methylsulfanyl]methanimidothioic acid

Identification

Molecular formula

C₁₄H₁₁Cl₂NS₂

CAS number

34562-65-1

IUPAC name

N-(3-chlorophenyl)-1-[(4-chlorophenyl)methylsulfanyl]methanimidothioic acid

State

This compound is usually found in a solid state at room temperature. The solid is fairly stable and has a crystalline structure.

Melting point (Celsius)

160.00

Melting point (Kelvin)

433.15

Boiling point (Celsius)

350.00

Boiling point (Kelvin)

623.15

General information

Molecular weight

295.76g/mol

Molar mass

295.7640g/mol

Density

1.4000g/cm³

Appearence

This is a crystalline compound that typically appears as a colorless or white solid, but may have tinges of color based on impurities or specific crystalline structures.

Comment on solubility

Solubility of N-(3-chlorophenyl)-1-[(4-chlorophenyl)methylsulfanyl]methanimidothioic acid

The solubility of N-(3-chlorophenyl)-1-[(4-chlorophenyl)methylsulfanyl]methanimidothioic acid presents an interesting case. Its unique structure, characterized by the presence of chlorophenyl groups and a thiol functional group, influences its solubility profile in various solvents. Here are some key points regarding its solubility:

Polar Solvents: The presence of the thiol group can enhance solubility in polar solvents like water and ethanol due to the formation of hydrogen bonds.
Non-Polar Solvents: Conversely, the chlorophenyl groups may limit solubility in non-polar solvents such as hexane. This structural characteristic can often lead to a lower affinity for non-polar environments.
pH Dependence: The solubility might vary with pH; at higher or lower pH conditions, ionization of the functional groups can occur, potentially increasing solubility.
Temperature Influence: Increasing temperature generally promotes solubility, making this compound potentially more soluble in warm solvents.

In summary, the solubility of N-(3-chlorophenyl)-1-[(4-chlorophenyl)methylsulfanyl]methanimidothioic acid is a complex interaction of its chemical structure and the properties of the solvent. Understanding these nuances is essential for applications in various chemical processes.

Interesting facts

Interesting Facts about N-(3-chlorophenyl)-1-[(4-chlorophenyl)methylsulfanyl]methanimidothioic acid

N-(3-chlorophenyl)-1-[(4-chlorophenyl)methylsulfanyl]methanimidothioic acid, commonly referred to as a thioamide compound, is a fascinating chemical with a range of applications and structural characteristics that make it noteworthy in the world of chemistry.

Unique Structural Features

Thioamide Group: The presence of the thioamide functional group contributes to its unique reactivity and properties, making it an interesting subject for studying reaction mechanisms.
Chlorinated Phenyl Moieties: With two chlorophenyl groups, this compound exhibits enhanced lipophilicity, which can influence its interactions with biological systems.

Applications and Research

This compound has attracted attention for its potential in various fields:

Pharmaceutical Development: Investigations into its pharmacological properties suggest it may have therapeutic applications.
Agricultural Research: The thioamide structure may impart herbicidal or fungicidal properties, paving the way for novel agrochemicals.
Material Science: As scientists explore its interaction with polymers and other materials, its unique sulfur-containing structure may provide new insights into composite materials.

Noteworthy Reactions

Additionally, N-(3-chlorophenyl)-1-[(4-chlorophenyl)methylsulfanyl]methanimidothioic acid serves as a precursor for numerous organic synthesis routes, and its reactivity can be manipulated in a variety of ways, leading to:

Formation of new thioamide derivatives, which may exhibit enhanced bioactivity.
Participation in condensation reactions that can yield diverse chemical architectures.

As you delve deeper into the properties and implications of this compound, remember: "In every molecule lies the potential for discovery." The exploration of its various facets not only enriches our understanding of thioamides but also underscores the importance of continued research in organic chemistry.