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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
State
State

At room temperature, the compound is expected to be a solid, possibly in a crystalline form due to its complex aromatic structure and molecular weight. The exact nature of its crystalline structure would depend on its synthesis and purification methods.

Melting point (Celsius)
146.88
Melting point (Kelvin)
420.03
Boiling point (Celsius)
489.30
Boiling point (Kelvin)
762.45
General information
Molecular weight
286.80g/mol
Molar mass
286.7990g/mol
Density
1.3083g/cm3
Appearence

The compound is likely a crystalline solid powders due to its organic nature. The presence of multiple functional groups including thioamide and ethoxycarbonylsulfanyl suggests it could have a distinctive color, potentially off-white to pale yellow, but exact color data may not be readily available.

Comment on solubility

Solubility of N-(4-chloro-3-methyl-phenyl)-1-ethoxycarbonylsulfanyl-methanimidothioic acid

N-(4-chloro-3-methyl-phenyl)-1-ethoxycarbonylsulfanyl-methanimidothioic acid is a compound that exhibits varying degrees of solubility, influenced by several factors including polarity, temperature, and pH. Here are some interesting insights into its solubility characteristics:

  • Polarity: The presence of both polar and non-polar functional groups affects how this compound interacts with solvents. Generally, polar solvents (like water) can dissolve polar substances better.
  • Temperature: Solubility can increase with temperature, depending on the compound's endothermic or exothermic dissolution process.
  • pH Sensitivity: Since the compound contains acidic groups, its solubility can be altered significantly by the pH of the solution. In basic conditions, ionization may improve solubility.

In summary, while specific data on solubility may vary, understanding these influencing factors is crucial for determining how N-(4-chloro-3-methyl-phenyl)-1-ethoxycarbonylsulfanyl-methanimidothioic acid behaves in different solvent environments. As the popular saying goes, "Like dissolves like," which highlights the importance of selecting the right solvent for optimal solubility.

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.