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Thiopental

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Identification
Molecular formula
C11H18N2O2S
CAS number
76-75-5
IUPAC name
5-ethyl-5-(2-methylallyl)-2-sulfanyl-1H-pyrimidine-4,6-dione
State
State

At room temperature, thiopental in its sodium salt form is a solid.

Melting point (Celsius)
158.00
Melting point (Kelvin)
431.15
Boiling point (Celsius)
313.60
Boiling point (Kelvin)
586.80
General information
Molecular weight
242.34g/mol
Molar mass
242.3190g/mol
Density
1.2974g/cm3
Appearence

Thiopental appears as a white crystalline powder with no odor. It is commonly encountered in its sodium salt form, which is soluble in water.

Comment on solubility

Solubility of 5-ethyl-5-(2-methylallyl)-2-sulfanyl-1H-pyrimidine-4,6-dione

The solubility of 5-ethyl-5-(2-methylallyl)-2-sulfanyl-1H-pyrimidine-4,6-dione can be quite complex due to its intricate molecular structure. Understanding the factors that influence its solubility is essential:

  • Polarity: The presence of the sulfur atom (*-S-* group) and various functional groups can alter the polarity of the compound, affecting how well it interacts with solvents.
  • Hydrogen Bonding: This compound can participate in hydrogen bonding, which may enhance its solubility in polar solvents like water.
  • Solvent Selection: The solubility can vary significantly across solvents. Common organic solvents like ethanol or acetone may dissolve the compound better than non-polar solvents.

Additionally, it is important to consider the influence of temperature and pressure on solubility. Generally, solubility tends to increase with temperature, but this behavior can vary based on the specific interactions within the compound.

In conclusion, while it may not be straightforward to predict the solubility of 5-ethyl-5-(2-methylallyl)-2-sulfanyl-1H-pyrimidine-4,6-dione, understanding its structural attributes allows for a better grasp of its solubility behavior in different environments.

Interesting facts

Interesting Facts About 5-ethyl-5-(2-methylallyl)-2-sulfanyl-1H-pyrimidine-4,6-dione

5-ethyl-5-(2-methylallyl)-2-sulfanyl-1H-pyrimidine-4,6-dione is a fascinating compound that belongs to the pyrimidine family, which is known for its diverse biological activities and applications in pharmacology and biochemistry. Here are some interesting aspects of this compound:

  • Structural Complexity: The compound features a distinctive pyrimidine ring with sulfur and ethyl groups, making it an interesting subject of study for chemists interested in heterocyclic compounds.
  • Biological Importance: Pyrimidine derivatives are significant in the field of medicinal chemistry as they can act as precursors for nucleic acids and influence various metabolic pathways.
  • Diverse Applications: Compounds like 5-ethyl-5-(2-methylallyl)-2-sulfanyl-1H-pyrimidine-4,6-dione are often investigated for their potential uses in developing pharmaceuticals, specifically in cancer and antiviral therapies.
  • Synthetic Routes: The synthesis of this compound involves various organic reactions, which can provide insights into methods of creating complex organic molecules efficiently.
  • Research Potential: Ongoing research into compounds of this nature can lead to the discovery of new biological activities, opening doors for novel treatments and applications.

In the words of chemist Linus Pauling, "The best way to have a good idea is to have a lot of ideas." Exploring compounds like 5-ethyl-5-(2-methylallyl)-2-sulfanyl-1H-pyrimidine-4,6-dione exemplifies the spirit of innovation and discovery in the world of chemistry. As researchers delve deeper into its properties, new applications can emerge, showcasing the compound's potential impact on science and health.