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2-Phenylethyliminomethanedithiol

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Identification
Molecular formula
C9H11NS2
CAS number
2885-00-9
IUPAC name
2-phenylethyliminomethanedithiol
State
State

At room temperature, 2-Phenylethyliminomethanedithiol is commonly in a solid state. It should be stored in airtight conditions to prevent oxidation which might alter its physical properties.

Melting point (Celsius)
57.00
Melting point (Kelvin)
330.15
Boiling point (Celsius)
332.20
Boiling point (Kelvin)
605.35
General information
Molecular weight
202.33g/mol
Molar mass
202.3270g/mol
Density
1.1411g/cm3
Appearence

2-Phenylethyliminomethanedithiol typically appears as a crystalline solid or powder. It can be characterized by its distinct aromatic odor, typical of compounds containing phenyl groups. The appearance can vary from white to pale yellow depending on the purity and specific form in which it is prepared.

Comment on solubility

Solubility of 2-phenylethyliminomethanedithiol

2-phenylethyliminomethanedithiol, a compound featuring multiple functional groups, exhibits intriguing solubility characteristics. The solubility of this compound can be influenced by various factors such as:

  • Polar Nature: The presence of thiol groups (-SH) contributes to polarity, which can increase its solubility in polar solvents such as water and alcohols.
  • Hydrophobic Interactions: The phenyl group introduces a hydrophobic character, making 2-phenylethyliminomethanedithiol less soluble in nonpolar solvents.
  • pH Dependency: The solubility may vary with changes in pH due to protonation/deprotonation of the thiol groups.

In general, this compound is expected to be soluble in polar aprotic solvents, while demonstrating lower solubility in non-polar solvents. It is crucial to note that the exact solubility can also be affected by temperature and the presence of a solubilizing agent. As always, when dealing with such compounds, experimentation is the best approach to accurately characterize solubility.

Interesting facts

Interesting Facts About 2-phenylethyliminomethanedithiol

2-phenylethyliminomethanedithiol is a fascinating compound with a unique structure and applications. This molecule exemplifies the rich diversity found within organic chemistry, showcasing how slight modifications in molecular structure can lead to varied chemical behaviors and properties.

Key Features:

  • Dual Functionalities: The presence of both imine and dithiol groups in its structure makes this compound particularly versatile. These functionalities often allow for reactions that can serve as intermediates in organic synthesis.
  • Biological Relevance: Compounds like 2-phenylethyliminomethanedithiol can play important roles in biological systems. They may exhibit antioxidant properties or interact with biological molecules, highlighting their potential utility in pharmaceuticals.
  • Potential Applications: Its unique structure positions it for use in several applications, including:
    • As a ligand in coordination chemistry, which can bind to metal ions.
    • In the formulation of sensors that detect specific ions or small molecules.
    • As a reagent in organic synthesis, aiding in the construction of more complex molecules.

Scientific Interest:

The study of 2-phenylethyliminomethanedithiol reveals important insights about molecular behavior in various environments and can enhance our understanding of chemical reactivity. As noted by many chemists, 'Embracing complexity often yields the most interesting discoveries.' This compound stands out as a prime example of how intricate molecular designs can lead to innovative applications.

In conclusion, dive deeper into the study of 2-phenylethyliminomethanedithiol, and you may uncover new pathways in both synthetic chemistry and biological research!