Skip to main content

Tiodonium

ADVERTISEMENT
Identification
Molecular formula
C11H18N2O2S2
CAS number
67841-86-5
IUPAC name
5-(1-methylbutyl)-5-(2-methylsulfanylethyl)-2-sulfanyl-1H-pyrimidine-4,6-dione
State
State

At room temperature, Tiodonium is a solid. It is stable under normal conditions and is insoluble in water.

Melting point (Celsius)
200.00
Melting point (Kelvin)
473.00
Boiling point (Celsius)
300.00
Boiling point (Kelvin)
573.00
General information
Molecular weight
272.39g/mol
Molar mass
272.3930g/mol
Density
1.3400g/cm3
Appearence

Tiodonium appears as an off-white to light yellow crystalline powder. The substance is typically dry and may appear clumpy or as fine granules.

Comment on solubility

Solubility Characteristics of 5-(1-methylbutyl)-5-(2-methylsulfanylethyl)-2-sulfanyl-1H-pyrimidine-4,6-dione

The solubility of a chemical compound is crucial in understanding its behavior in various environments and applications. For the compound 5-(1-methylbutyl)-5-(2-methylsulfanylethyl)-2-sulfanyl-1H-pyrimidine-4,6-dione, several factors influence its solubility:

  • Polarity: The presence of functional groups and the molecular structure plays a vital role in determining the compound's polarity, which in turn affects its solubility in polar and non-polar solvents.
  • Temperature: Generally, the solubility of organic compounds can increase with temperature. Hence, it is essential to assess solubility under varying thermal conditions.
  • pH Sensitivity: If the compound contains acidic or basic functional groups, its solubility may vary significantly with changes in pH.
  • Solvent Choice: The nature of the solvent is critical. For example, this compound may be more soluble in organic solvents like ethanol or dimethyl sulfoxide (DMSO) rather than in water.

In summary, the solubility of 5-(1-methylbutyl)-5-(2-methylsulfanylethyl)-2-sulfanyl-1H-pyrimidine-4,6-dione depends on its chemical structure and the conditions under which it is being evaluated. Understanding these nuances is essential for optimizing its use in various chemical processes.

Interesting facts

Interesting Facts about 5-(1-methylbutyl)-5-(2-methylsulfanylethyl)-2-sulfanyl-1H-pyrimidine-4,6-dione

This unique compound is part of the pyrimidine family, known for its wide range of biological activities and applications in medicinal chemistry. Here are some intriguing aspects to consider:

  • Pharmacological Potential: The structural variations in the pyrimidine ring make it a versatile scaffold for designing pharmaceuticals. Researchers have investigated similar compounds for their potential as antitumor, antiviral, and anti-inflammatory agents.
  • Sulfur Importance: The presence of sulfur-containing groups is significant as they often enhance the biological properties of compounds. This compound includes thiol groups, which may contribute to its reactivity and interactions in biological systems.
  • Structure-Activity Relationship (SAR): Understanding how modifications to the molecular structure affect biological activity is crucial. In this molecule, the branched alkyl groups could influence solubility and activity, revealing the importance of SAR studies in drug development.
  • Natural Analogues: Compounds related to this chemical structure can be found in various natural products. This highlights the remarkable diversity in nature, where different compounds can exhibit similar biological actions.
  • Research Interest: Due to its complex structure, studies on this compound can provide insights into synthetic methodologies and chemistry. It can serve as a model for future research on new derivatives that could exhibit enhanced biological properties.

In the world of chemistry, 5-(1-methylbutyl)-5-(2-methylsulfanylethyl)-2-sulfanyl-1H-pyrimidine-4,6-dione stands as a testament to the intricate relationship between structure and function. As researchers continue to explore its characteristics, we may uncover novel applications and deeper biochemical insights.