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Thiazolidine-2-thione

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Identification
Molecular formula
C3H5NS
CAS number
616-19-3
IUPAC name
3,4-dihydro-2H-pyrrole-5-thiol
State
State

At room temperature, Thiazolidine-2-thione is in the solid state. It is typically stable and maintains its structure under standard conditions.

Melting point (Celsius)
68.00
Melting point (Kelvin)
341.00
Boiling point (Celsius)
219.00
Boiling point (Kelvin)
492.00
General information
Molecular weight
103.17g/mol
Molar mass
103.1680g/mol
Density
1.2000g/cm3
Appearence

Thiazolidine-2-thione appears as a white to off-white crystalline solid at room temperature. The compound has a subtle sulfurous odor due to the presence of the thiol group.

Comment on solubility

Solubility of 3,4-Dihydro-2H-pyrrole-5-thiol

The solubility characteristics of 3,4-dihydro-2H-pyrrole-5-thiol can be quite intriguing due to its unique chemical structure. As a thiol compound, it presents specific solubility properties that are important to understand:

  • Water Solubility: 3,4-dihydro-2H-pyrrole-5-thiol is expected to exhibit moderate solubility in water. This is due to the presence of the thiol (-SH) group, which can form hydrogen bonds with water molecules.
  • Organic Solvents: The compound may show greater solubility in various organic solvents such as ethanol and acetone. This is attributed to its hydrophobic regions that interact favorably with non-polar substances.
  • Influence of pH: The solubility can also be affected by the pH of the solution. Under acidic conditions, the protonation of the thiol group can modify its solubility profile.
  • Temperature Dependency: As with many organic compounds, increasing the temperature may enhance solubility, as higher temperatures generally increase molecular movement and solubility rates.

In summary, the solubility of 3,4-dihydro-2H-pyrrole-5-thiol is influenced by its thiol functional group and hydrophobic properties. Understanding these factors is crucial for its applications in various chemical contexts.

Interesting facts

Interesting Facts about 3,4-dihydro-2H-pyrrole-5-thiol

3,4-Dihydro-2H-pyrrole-5-thiol is a fascinating organic compound that belongs to the class of heterocyclic compounds. Often discussed in the context of organic synthesis, this molecule exhibits unique properties due to its thiol group and pyrrole structure. Here are some interesting insights:

  • Heterocyclic Structure: The pyrrole ring is a five-membered aromatic ring containing nitrogen, contributing to the compound's chemical reactivity and stability.
  • Thiol Group: This particular compound features a thiol (-SH) functional group, which enhances its potential for forming disulfide bonds and participating in various redox reactions.
  • Biological Relevance: Compounds with thiol groups are often found in biological systems, playing significant roles in enzyme function and protein structure stabilization.
  • Synthetic Versatility: 3,4-Dihydro-2H-pyrrole-5-thiol is noteworthy for its potential use in the synthesis of more complex natural products and pharmaceuticals.
  • Research Focus: The compound has garnered attention in recent studies for its potential implications in medicinal chemistry, particularly as an antioxidant.

Scientists often emphasize the intriguing chemistry of thiol-containing compounds, given their reactivity and ability to interact with various biological molecules. As the world of synthetic organic chemistry continues to evolve, 3,4-dihydro-2H-pyrrole-5-thiol remains a compound of interest, offering numerous possibilities for exploration and discovery.