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
Molecular Weight
345.80g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
2.1500g/cm3
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.

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