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Identification

Molecular formula
C11H12ClNO2S2
CAS Number
915488-17-4
IUPAC Name
N-(4-chloro-3-methyl-phenyl)-1-ethoxycarbonylsulfanyl-methanimidothioic acid
Molecular Weight
286.80g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.3083g/cm3
Interesting facts

Interesting Facts about N-(4-chloro-3-methyl-phenyl)-1-ethoxycarbonylsulfanyl-methanimidothioic acid

N-(4-chloro-3-methyl-phenyl)-1-ethoxycarbonylsulfanyl-methanimidothioic acid is a fascinating compound that opens up discussions on various fronts, particularly in medicinal chemistry and sulfur chemistry. Here are some notable highlights:

  • Dual Functionalities: This compound features both thioic and carbonyl functionalities, which enable it to participate in a wide array of chemical reactions, making it crucial for synthetic applications.
  • Medicinal Potential: Compounds with thioic acid derivatives have shown potential in pharmaceutical applications, particularly as they may display antimicrobial, antiviral, or anticancer properties.
  • Sulfur Chemistry: The presence of sulfur in its structure highlights the importance of thiols and thioacids in organic synthesis. These compounds can serve as nucleophiles due to sulfur’s unique electronic properties.
  • Chiral Influences: The asymmetrical carbon surrounding the carbonyl functionality may lead to enantiomeric forms, which could have different biological activities, hinting at the importance of chirality in drug design.
  • Environmental Impact: Understanding the reactivity of such compounds also plays a significant role in environmental chemistry, as some derivatives may interact with biological systems or pollutants.

As a scientist or student delving into this compound, one might ponder: How can modifications to its structure enhance its activity? This question invites further exploration into structure-activity relationships (SAR) and encourages an investigative mindset into the world of organic chemistry.

In conclusion, N-(4-chloro-3-methyl-phenyl)-1-ethoxycarbonylsulfanyl-methanimidothioic acid not only serves as an interesting case study in chemical synthesis but also as a gateway to broader themes in medicinal chemistry, environmental science, and sulfur chemistry.

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