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1-Phenylethyliminomethanedithiol

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Identification
Molecular formula
C10H13NS2
CAS number
79555-37-8
IUPAC name
1-phenylethyliminomethanedithiol
State
State

At room temperature, 1-Phenylethyliminomethanedithiol exists as a liquid.

Melting point (Celsius)
-10.00
Melting point (Kelvin)
263.15
Boiling point (Celsius)
138.00
Boiling point (Kelvin)
411.15
General information
Molecular weight
198.34g/mol
Molar mass
198.3400g/mol
Density
1.1400g/cm3
Appearence
The compound 1-Phenylethyliminomethanedithiol is typically found in a liquid state and can exhibit a pale yellow color. Due to its thiol content, it may have a characteristic unpleasant odor typical of sulfur-containing compounds.
Comment on solubility

Solubility of 1-phenylethyliminomethanedithiol

The solubility of 1-phenylethyliminomethanedithiol is influenced by several factors that determine its behavior in various solvents.

Here are some key considerations regarding its solubility:

  • Polarity: The compound has polar functional groups, which generally enhance solubility in polar solvents like water and alcohols.
  • Hydrogen Bonding: The presence of thiol groups (-SH) suggests that 1-phenylethyliminomethanedithiol can engage in hydrogen bonding, potentially increasing its solubility in aqueous environments.
  • Hydrophobic Interactions: The phenyl group contributes hydrophobic characteristics, which may reduce solubility in water but could enhance solubility in non-polar organic solvents.

As a general observation, one might say:

"The solubility of a compound is a dance between its polar and non-polar features, with each solvent playing its own unique tune."

In trials, this compound may show a tendency to dissolve effectively in solvents that can stabilize its unique structure, particularly in organic solvents or mixed solvent systems. The understanding of such solubility characteristics is crucial for practical applications and further research.

Interesting facts

Interesting Facts about 1-Phenylethyliminomethanedithiol

1-Phenylethyliminomethanedithiol is a fascinating compound that finds its applications in various fields of chemistry and materials science. Here are some intriguing details about this compound:

  • Structure and Composition: The compound features a unique structure that combines an imino group with a dithiol functionality. This combination equips it with unique properties, making it an interesting subject for study.
  • Applications in Coordination Chemistry: Due to the presence of thiol (-SH) groups, this compound can readily form coordination complexes with transition metals. These complexes can possess unique catalytic properties or enhance biological functionalities.
  • Potential Biological Relevance: Compounds with thiol groups are known for their role in biological systems, such as participating in enzyme activity and cellular defense mechanisms. The study of 1-phenylethyliminomethanedithiol might reveal insights into its biological implications.
  • Research in Organic Synthesis: Chemists often explore such compounds for innovative organic synthesis methods, potentially leading to the development of new drugs or materials. The flexibility of its functional groups allows for diverse synthetic pathways.
  • Stability Examination: The stability of thiols under varying conditions is a recognized area of study. Investigating the stability of 1-phenylethyliminomethanedithiol can offer chemists a better understanding of how similar compounds behave in different environments.

In summary, 1-phenylethyliminomethanedithiol is not just a mere combination of atoms; it is a significant chemical entity that could pave the way for advancements in multiple scientific fields. The exploration of its properties and implications continues to excite both established scientists and newcomers in the chemical community.