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Imominomethanedithiol

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Identification
Molecular formula
C2H3NS2
CAS number
32578-13-7
IUPAC name
iminomethanedithiol
State
State

At room temperature, iminomethanedithiol is typically in its solid state. It is relatively stable in this form but should be handled under controlled conditions as it might be reactive with other substances.

Melting point (Celsius)
36.00
Melting point (Kelvin)
309.15
Boiling point (Celsius)
120.50
Boiling point (Kelvin)
393.65
General information
Molecular weight
94.17g/mol
Molar mass
94.1700g/mol
Density
1.3500g/cm3
Appearence

Imominomethanedithiol is a yellow crystalline solid with a distinctive odor. It has a granular or powdery texture and can appear slightly oily to the touch. Under different lighting conditions, the color may vary slightly but it remains within the yellow spectrum.

Comment on solubility

Solubility of Iminomethanedithiol

Iminomethanedithiol, with the chemical formula H2NCH2CS2H, presents interesting characteristics regarding its solubility. Understanding the solubility of this compound is crucial, especially in applications involving chemical reactions and formulations.

Here are some key points regarding its solubility:

  • Polar Nature: The presence of amino (–NH2) and thiol (–SH) groups contributes to a certain degree of polarity in iminomethanedithiol, enabling it to interact with polar solvents.
  • Water Solubility: This compound is likely to be soluble in water due to its polar functional groups, which can form hydrogen bonds with water molecules.
  • Solvent Versatility: Iminomethanedithiol might also be soluble in various organic solvents; however, the specific solubility can depend on factors such as temperature and solvent characteristics.
  • Practical Considerations: When working with iminomethanedithiol, it's important to carefully assess its solubility in the intended solvent system for applications in reaction chemistry or material synthesis.

In summary, the solubility of iminomethanedithiol is influenced by its chemical structure and the nature of the solvent used. As with many compounds, experimental data is essential for confirming solubility behavior in specific conditions.

Interesting facts

Exploring Iminomethanedithiol

Iminomethanedithiol, commonly referred to as a thiol compound, offers a fascinating perspective for both chemists and students interested in organic chemistry. This compound is notable for its unique structure, which features both amine and thiol functional groups. Here are some intriguing facts:

  • Dual Functionalities: The presence of both an imine and a thiol group allows for versatile reactivity. This makes iminodithiols important in various organic synthesis processes.
  • Biological Relevance: Compounds with thiol groups are often involved in biological systems. They play crucial roles in protein structure and function, serving as redox-active sites and influencing enzyme activity.
  • Coordination Chemistry: Iminomethanedithiol can serve as a ligand in coordination complexes, effectively binding to metal ions. This facilitates further exploration in the field of materials science and catalysis.
  • Potential Applications: With unique properties arising from its functional groups, iminomethanedithiol could have opportunities in drug development, specifically in the design of therapeutics that target specific biomolecular interactions.
  • Research Interest: This compound has garnered interest in various fields, including environmental chemistry and agriculture, particularly for its potential applications in chelation and detoxification of heavy metals.

As a student or researcher delving into the world of organic compounds, the study of iminomethanedithiol opens avenues to explore innovative chemical reactions and their implications in real-world applications. Its complex chemical behavior makes it a valuable subject for further investigation and experimentation.