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Thiohydantoin

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Identification
Molecular formula
C8H7NOS
CAS number
23713-54-8
IUPAC name
3-sulfanylisoindol-1-one
State
State

At room temperature, 3-sulfanylisoindol-1-one is generally in a solid state.

Melting point (Celsius)
239.15
Melting point (Kelvin)
512.30
Boiling point (Celsius)
453.15
Boiling point (Kelvin)
726.30
General information
Molecular weight
149.19g/mol
Molar mass
149.1940g/mol
Density
1.5340g/cm3
Appearence

3-Sulfanylisoindol-1-one typically appears as a colorless to pale yellow crystalline solid.

Comment on solubility

Solubility of 3-sulfanylisoindol-1-one

When discussing the solubility of 3-sulfanylisoindol-1-one, it's important to consider several factors that influence its behavior in various solvents. This compound, with the molecular formula C8H7N1O1S1, exhibits some intriguing characteristics:

  • Polarity: The presence of a sulfanyl group can enhance the polarity of the molecule, suggesting that it may be more soluble in polar solvents like water.
  • Hydrogen Bonding: The potential for hydrogen bonding due to the amide-like structure can further influence its solubility profile.
  • Solvents: It is expected to be moderately soluble in common organic solvents such as ethanol and dimethyl sulfoxide (DMSO) due to its somewhat polar nature.
  • Temperature Effects: As with many organic compounds, solubility may increase with temperature, allowing for greater solute interactions in solution.

To summarize, while 3-sulfanylisoindol-1-one may not dissolve extensively in non-polar solvents, its solubility is likely enhanced in polar environments and with increased temperature, making it a compound of interest for further studies on solvent interactions.

Interesting facts

Interesting Facts about 3-sulfanylisoindol-1-one

3-sulfanylisoindol-1-one is a fascinating compound that intersects various fields of chemistry, biology, and materials science. Here are some notable aspects to explore:

  • Chemical Structure: This compound features an isoindole core, which is a bicyclic structure known for its unique electronic properties. The incorporation of a sulfanyl (-SH) group enhances its reactivity and potential applications.
  • Biological Relevance: Compounds with isoindole scaffolds have been studied for their biological activities, including potential antitumor and anti-inflammatory effects. Researchers are keen to investigate how 3-sulfanylisoindol-1-one may interact with biological systems.
  • Research Applications: Its structural uniqueness provides a valuable template for the design of novel pharmaceuticals and agrochemicals. The compound may also serve as a probe in studying various chemical and biological processes.
  • Reaction Chemistry: 3-sulfanylisoindol-1-one can participate in diverse chemical reactions, including nucleophilic substitutions and reductions, making it a versatile building block for organic synthesis.
  • Potential in Materials Science: The presence of the sulfur atom may impart interesting properties that could be harnessed in developing polymeric materials or as stabilizers in chemical formulations.

As they say in chemistry, "the power of understanding is rooted in the complexity of structure." The exploration of compounds like 3-sulfanylisoindol-1-one opens doors to new discoveries and innovations in both the academic and practical realms of science.