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2-Mercaptothiazoline

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Identification
Molecular formula
C3H5NOS2
CAS number
96-53-7
IUPAC name
2-sulfanylthiazol-4-one
State
State

2-Mercaptothiazoline is in a solid state at room temperature. Its crystalline structure and pale coloration make it identifiable among other solid organic compounds.

Melting point (Celsius)
96.50
Melting point (Kelvin)
369.70
Boiling point (Celsius)
344.10
Boiling point (Kelvin)
617.30
General information
Molecular weight
119.18g/mol
Molar mass
119.1830g/mol
Density
1.4420g/cm3
Appearence

2-Mercaptothiazoline typically appears as a white to pale yellow crystalline solid. Its presence can also be identified by a distinctive, somewhat unpleasant smell that is often associated with sulfur-containing compounds.

Comment on solubility

Solubility of 2-sulfanylthiazol-4-one

2-sulfanylthiazol-4-one, known for its intriguing structure and biological properties, exhibits unique solubility characteristics. Understanding its solubility can shed light on its potential applications and interactions.

Key Points on Solubility:

  • Water Solubility: 2-sulfanylthiazol-4-one shows limited solubility in water, indicating that it is likely to be more soluble in organic solvents.
  • Solvent Compatibility: The compound is known to dissolve well in polar organic solvents such as methanol and dimethyl sulfoxide (DMSO), which can enhance its usability in various chemical reactions.
  • Influence of pH: The solubility may also be affected by the pH of the solution, as ionization can play a crucial role in the dissolution process.

As quoted by chemists, "The solubility of a compound is a gateway to its chemical behavior and reactivity." This emphasizes the importance of studying the solubility dynamics of 2-sulfanylthiazol-4-one to harness its potential in pharmaceutical and industrial applications.

In summary, while 2-sulfanylthiazol-4-one is not highly soluble in water, its solubility in organic solvents opens avenues for various chemical explorations and applications. Understanding these solubility traits is paramount for researchers working with this compound.

Interesting facts

Exploring 2-sulfanylthiazol-4-one

2-sulfanylthiazol-4-one, a fascinating compound, belongs to the thiazole family, which features a five-membered aromatic ring containing both sulfur and nitrogen. This compound is particularly interesting due to its unique structural elements and the functional groups it contains. Here are some noteworthy points:

  • Biological Significance: 2-sulfanylthiazol-4-one has garnered attention in medicinal chemistry for its potential antibacterial and antifungal properties. Compounds with a thiazole ring are often found in pharmaceuticals, contributing to their therapeutic effects.
  • Reactivity: The presence of the thiol (-SH) group in its structure makes this compound a potent nucleophile, which can engage in various chemical reactions. This behavior is foundational in organic synthesis, particularly in the development of new drugs.
  • Synthesis: The synthetic routes to obtain 2-sulfanylthiazol-4-one often involve straightforward condensation reactions, making it accessible for research and application. This ease of synthesis invites chemists to explore derivatives and analogs.
  • Role in Coordination Chemistry: Thiazole derivatives like 2-sulfanylthiazol-4-one can act as ligands in coordination complexes, enhancing the stability and reactivity of metal ions in various environments.

As noted by many researchers, "the versatility of thiazole derivatives in drug design and catalytic processes makes them invaluable in contemporary chemistry." The study of 2-sulfanylthiazol-4-one offers a window into the intriguing interplay between structure and function in chemical compounds, showcasing the potential applications of thiazole-related chemicals across multiple fields.