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Formamidine disulfide

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Identification
Molecular formula
C3H8N2S4
CAS number
13829-24-8
IUPAC name
2-[bis(sulfanyl)methyleneamino]ethyliminomethanedithiol
State
State

At room temperature, formamidine disulfide exists typically as a solid due to its crystalline nature. This state is stable under normal laboratory conditions and is common for compounds with higher molecular weights, like formamidine disulfide.

Melting point (Celsius)
120.00
Melting point (Kelvin)
393.15
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
154.27g/mol
Molar mass
154.2700g/mol
Density
0.0000g/cm3
Appearence

Formamidine disulfide is typically a pale yellow crystalline solid. Its appearance can vary slightly depending on its specific formulation and preparation method. The compound is usually crystalline when pure, and may appear slightly different if impurities are present.

Comment on solubility

Solubility of 2-[bis(sulfanyl)methyleneamino]ethyliminomethanedithiol

The solubility of 2-[bis(sulfanyl)methyleneamino]ethyliminomethanedithiol can be influenced by its unique chemical structure and the presence of various functional groups. Understanding its solubility characteristics is essential when considering its applications. Here are some important points to consider:

  • Polarity: The presence of sulfanyl (-SH) groups and amino (-NH2) functionality may increase its polarity, which can enhance solubility in polar solvents like water.
  • Hydrogen Bonding: The ability of this compound to form hydrogen bonds with solvents contributes to its solubility. Compounds capable of strong hydrogen bonding typically exhibit higher solubility in water.
  • Solvent Compatibility: It is likely to be more soluble in alcohols and other polar organic solvents due to its functional groups.
  • Concentration: As with many compounds, the solubility may depend on concentration levels, temperature, and the pH of the solution.

In summary, while specific solubility values may vary, the polar nature and functional characteristics of 2-[bis(sulfanyl)methyleneamino]ethyliminomethanedithiol suggest that it should exhibit reasonable solubility in polar solvents, making it versatile for various chemical interactions and applications.

Interesting facts

Interesting Facts about 2-[bis(sulfanyl)methyleneamino]ethyliminomethanedithiol

This fascinating compound, known for its unique structure and sulfur-centered chemistry, has quickly gained interest among researchers and chemists alike. Its complexity comes from the presence of multiple functional groups, particularly the sulfur and nitrogen functionalities, which can influence its reactivity and interaction with various systems.

Key Characteristics

  • Multifunctionality: The compound contains both thiol (-SH) groups and an imine functionality, allowing it to participate in diverse chemical reactions such as condensation and thiol-disulfide exchange.
  • Potential Applications: This compound may have promising applications in fields such as drug development, materials science, and bioengineering due to its unique reactivity.
  • Sulfur Chemistry: With sulfur playing a crucial role in biochemistry, studying this compound could yield insights into sulfur's biological functions, including its role in enzyme activity and antioxidant processes.

Moreover, as noted by many chemists, "the intricate lattice of interactions in such compounds offers a wealth of research opportunities." From a synthetic perspective, the ability to manipulate its structure opens doors to developing tailored derivatives with specific properties.

Research Potential

Understanding the behavior of 2-[bis(sulfanyl)methyleneamino]ethyliminomethanedithiol could lead to significant advancements in the following areas:

  1. Catalysis: Its ability to undergo varied transformations makes it a candidate for catalyzing important organic reactions.
  2. Medicinal Chemistry: Investigating the medicinal properties of sulfur-containing compounds could pave the way for novel therapeutic agents.
  3. Material Science: Potential applications in developing materials with enhanced electrical or optical properties.

In conclusion, as scientists delve deeper into the realm of this compound, they uncover layers of potential that connect it to broader applications in chemistry and beyond. The continued study of 2-[bis(sulfanyl)methyleneamino]ethyliminomethanedithiol is not just about understanding a single compound but represents the ongoing quest for knowledge in chemical sciences.