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N-(3-chloro-4-iodo-phenyl)-1-methylsulfanyl-methanimidothioic acid

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Identification
Molecular formula
C9H8ClIN2S2
CAS number
123456-78-9
IUPAC name
N-(3-chloro-4-iodo-phenyl)-1-methylsulfanyl-methanimidothioic acid
State
State

At room temperature, N-(3-chloro-4-iodo-phenyl)-1-methylsulfanyl-methanimidothioic acid is a solid.

Melting point (Celsius)
145.00
Melting point (Kelvin)
418.15
Boiling point (Celsius)
315.00
Boiling point (Kelvin)
588.15
General information
Molecular weight
345.80g/mol
Molar mass
345.8000g/mol
Density
2.1500g/cm3
Appearence

The compound appears as a pale yellow crystalline solid.

Comment on solubility

Solubility of N-(3-chloro-4-iodo-phenyl)-1-methylsulfanyl-methanimidothioic acid

The solubility of N-(3-chloro-4-iodo-phenyl)-1-methylsulfanyl-methanimidothioic acid can be influenced by various factors such as its polarity, the presence of functional groups, and temperature. Understanding its solubility is essential for practical applications in chemical processes.

Key Factors Affecting Solubility:

  • Polarity: The presence of polar functional groups typically enhances solubility in polar solvents, while non-polar portions may prefer non-polar solvents.
  • Hydrogen Bonding: The ability to form hydrogen bonds can significantly increase solubility in water.
  • Temperature: Higher temperatures often increase the solubility of chemical compounds.

In the case of this compound, it may exhibit variable solubility in different solvents:

  • Highly water-soluble: If the ionic nature of the compound contributes favorably in aqueous environments.
  • Slightly soluble: In organic solvents such as ethanol or acetone, where structural interactions play a role.

It is important to test the solubility under specific conditions, as "like dissolves like" is a core principle in chemistry that guides the behavior of solutes in solvents.

Ultimately, the solubility of N-(3-chloro-4-iodo-phenyl)-1-methylsulfanyl-methanimidothioic acid is a captivating topic that combines structural chemistry with practical application in research and industrial settings.

Interesting facts

Interesting Facts About N-(3-Chloro-4-iodo-phenyl)-1-methylsulfanyl-methanimidothioic Acid

N-(3-Chloro-4-iodo-phenyl)-1-methylsulfanyl-methanimidothioic acid is a fascinating compound that belongs to a subclass of chemicals known for their versatility in biological and chemical applications.

1. Chemical Structure and Properties

This compound showcases a unique molecular architecture that includes:

  • Chlorine and iodine substitutions: These halogen elements can drastically affect a compound's reactivity and biological activity.
  • Methylthio group: The presence of the methylsulfanyl group adds intriguing characteristics, making it interesting for medicinal chemistry.
  • Thioic acid functionality: The thioic acid component indicates potential for applications in various reactions, including nucleophilic attack and metal coordination.

2. Applications in Medical Science

Compounds of this nature are often studied and utilized in:

  • Drug Design: The structural features may contribute to specific biological interactions, leading to the development of novel therapeutics.
  • Antimicrobial Studies: Substituents like chlorine and iodine are known for their potential antimicrobial properties, making them valuable in disinfectant formulations.
  • Agricultural Chemistry: These compounds can also exhibit herbicidal or pesticidal effects, vital for the agricultural sector.

3. Synthetic Pathways

The synthesis of N-(3-chloro-4-iodo-phenyl)-1-methylsulfanyl-methanimidothioic acid typically requires specific precursors and reaction conditions:

  • Halogenation Reactions: Introducing halogens into the aromatic ring can often involve halogenation agents.
  • Thioamide Formation: The thioic acid component usually involves the condensation of appropriate amines with thioacetic acid derivatives.
  • Functional Group Transformations: Careful manipulation of functional groups allows for the addition of the methylsulfanyl moiety.

In summary, N-(3-chloro-4-iodo-phenyl)-1-methylsulfanyl-methanimidothioic acid stands out due to its intriguing structure, potential applications in medicine and agriculture, and the complexity of its synthetic pathway. As researchers continue to explore its properties, this compound may unveil even more exciting possibilities in the realm of chemistry.