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5-Methyl-2-thiouracil

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Identification
Molecular formula
C5H6N2OS
CAS number
1068-07-9
IUPAC name
5-methyl-2-sulfanyl-1H-pyrimidin-6-one
State
State

At room temperature, 5-Methyl-2-thiouracil is in a solid state, maintaining a stable form unless subjected to higher temperatures where it transitions through its melting and boiling points.

Melting point (Celsius)
288.00
Melting point (Kelvin)
561.15
Boiling point (Celsius)
412.00
Boiling point (Kelvin)
685.15
General information
Molecular weight
142.17g/mol
Molar mass
142.1720g/mol
Density
1.2930g/cm3
Appearence

5-Methyl-2-thiouracil is typically a pale yellow crystalline solid, characterized by its distinct crystal structure. It is unremarkable in terms of odor, presenting with a typical neutral scent expected of many pyrimidine derivatives.

Comment on solubility

Solubility of 5-methyl-2-sulfanyl-1H-pyrimidin-6-one

Understanding the solubility of 5-methyl-2-sulfanyl-1H-pyrimidin-6-one is essential for its applications in various fields. The solubility of a compound often depends on several factors, including its chemical structure, polarity, and the solvent used.

Key considerations for solubility include:

  • Chemical structure: The presence of functional groups in 5-methyl-2-sulfanyl-1H-pyrimidin-6-one can influence its solubility. The sulfhanyl group (-SH) may enhance solubility in polar solvents.
  • Polarity: This compound's polar nature can lead to higher solubility in polar solvents like water and alcohols.
  • Temperature: Increased temperature typically increases solubility; thus, solubility tests should be conducted at various temperatures for accurate readings.
  • pH levels: The solubility may vary depending on the acidity or basicity of the solution. Adjusting the pH can optimize solubility.

In summary, the solubility of 5-methyl-2-sulfanyl-1H-pyrimidin-6-one is influenced by its unique functional groups and overall structure, making it potentially more soluble in polar solvents. Evaluating these factors can provide valuable insights into its behavior in various chemical environments.

Interesting facts

Exploring 5-Methyl-2-sulfanyl-1H-pyrimidin-6-one

5-Methyl-2-sulfanyl-1H-pyrimidin-6-one is a fascinating compound that belongs to the pyrimidine family, a class of organic compounds notable for their aromatic properties and diverse biological activities. Pyrimidines are integral to numerous biochemical processes, making this compound a topic of interest in both medicinal chemistry and biochemistry.

Key Characteristics

  • Structural Features: The presence of both a methyl group and a sulfanyl group contributes to its unique reactivity and solubility profiles.
  • Biological Significance: Compounds like this one can interact with biological systems, potentially inhibiting enzymes or acting as substrates for metabolic pathways.
  • Applications: Research indicates that pyrimidine derivatives may have applications in the treatment of various diseases, including cancer and viral infections.

This compound also prompts interesting discussions surrounding its synthesis and functional groups. The sulfanyl group, in particular, has been noted for its role in enhancing the biological activity of certain pharmaceuticals. In the words of famous chemist Linus Pauling: "The best way to have a good idea is to have lots of ideas." Embracing the structural diversity of compounds like 5-methyl-2-sulfanyl-1H-pyrimidin-6-one opens up many avenues for research and discovery.

As we delve deeper into the world of organic chemistry, the study of such compounds illustrates the intricate relationship between structure, function, and application. Scientists continue to explore and optimize the properties of pyrimidine derivatives for innovative therapeutic solutions.