.
- 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
Identification
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.