Skip to main content

N-benzyl-1-methylsulfanyl-methanimidothioic acid

ADVERTISEMENT
Identification
Molecular formula
C9H11NS2
CAS number
2466-99-5
IUPAC name
N-benzyl-1-methylsulfanyl-methanimidothioic acid
State
State

At room temperature, N-benzyl-1-methylsulfanyl-methanimidothioic acid is typically found in the solid state.

Melting point (Celsius)
90.00
Melting point (Kelvin)
363.15
Boiling point (Celsius)
298.00
Boiling point (Kelvin)
571.15
General information
Molecular weight
205.33g/mol
Molar mass
205.3270g/mol
Density
1.1800g/cm3
Appearence

The compound N-benzyl-1-methylsulfanyl-methanimidothioic acid typically appears as a crystalline solid. The appearance can vary slightly based on purity and form, but it is usually colorless or light yellow.

Comment on solubility

Solubility of N-benzyl-1-methylsulfanyl-methanimidothioic acid

N-benzyl-1-methylsulfanyl-methanimidothioic acid, a compound with a complex structure, presents intriguing solubility characteristics. Its ability to dissolve in various solvents significantly depends on the functional groups present and their interactions with surrounding molecules. Here are some key points regarding its solubility:

  • Polarity: The presence of the methylsulfanyl group contributes to polar interactions, which may enhance solubility in polar solvents such as water or alcohols.
  • Hydrogen Bonding: The carboxylic acid functionality can engage in hydrogen bonding, further affecting solubility in protic solvents.
  • Solvent Type: This compound may show varying solubility in:
    • Polar solvents: High solubility due to interactions with water molecules.
    • Nonpolar solvents: Lower solubility, as the hydrophobic benzyl group may limit interaction with nonpolar environments.
  • Temperature Effects: As with many organic compounds, solubility generally increases with temperature, making it easier for the compound to interact with solvents in warmer conditions.

In conclusion, the solubility of N-benzyl-1-methylsulfanyl-methanimidothioic acid can be described as conditional, influenced by various factors including polarity, hydrogen bonding capabilities, and the nature of the solvent. Understanding these interactions is essential for applications involving this compound.

Interesting facts

Interesting Facts About N-benzyl-1-methylsulfanyl-methanimidothioic Acid

N-benzyl-1-methylsulfanyl-methanimidothioic acid is a fascinating compound with a variety of implications in the field of chemistry and beyond. Here are some intriguing insights:

  • Structure and Functionality: This compound features a unique structure that combines both thioic acid and sulfonamide functionalities. Such duality in functional groups allows for diverse chemical reactivity, which is a point of interest for synthetic chemists.
  • Applications in Medicine: Compounds similar to N-benzyl-1-methylsulfanyl-methanimidothioic acid may have potential medicinal applications. The thioic acid moiety can play a role in biochemical interactions, offering possibilities in drug design and development.
  • Synthesis Considerations: The synthesis of this compound typically requires careful control of reaction conditions. The presence of sulfur in the structure poses an interesting challenge regarding the conditions under which it can be produced effectively.
  • Research Opportunities: Given its unique chemical properties, this compound may serve as a useful template in research aimed at discovering new catalysts or pharmaceuticals. Exploring its reactivity could unveil new pathways for chemical synthesis.
  • Environmental Impact: Understanding the interactions and breakdown pathways of such sulfur-containing compounds in the environment is crucial for assessing their ecological footprints, particularly in agricultural chemistry.

In summary, N-benzyl-1-methylsulfanyl-methanimidothioic acid invites further exploration due to its complex structure and promising applications, making it a noteworthy compound in both organic chemistry and medicinal research.