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Tiapride

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Identification
Molecular formula
C10H15N2O2S2
CAS number
51012-32-9
IUPAC name
5-(butylsulfanylmethyl)-5-ethyl-2-sulfanyl-1H-pyrimidine-4,6-dione
State
State

At room temperature, Tiapride exists as a solid substance.

Melting point (Celsius)
193.00
Melting point (Kelvin)
466.00
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
314.46g/mol
Molar mass
314.4300g/mol
Density
1.3900g/cm3
Appearence

Tiapride generally appears as a crystalline powder that is white or almost white in color. It is typically available in solid form.

Comment on solubility

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

The solubility of 5-(butylsulfanylmethyl)-5-ethyl-2-sulfanyl-1H-pyrimidine-4,6-dione is primarily influenced by its chemical structure and the functional groups present. While specific solubility data may not be extensively documented, the following observations can be made:

  • Polarity: The presence of multiple sulfur-containing functional groups suggests a degree of polarity, which might enhance solubility in polar solvents.
  • Hydrophobic Characteristics: The butylsulfanyl group introduces hydrophobic characteristics, potentially limiting solubility in water but improving it in organic solvents.
  • General Trend: Compounds with heterocyclic structures can vary widely in solubility based on their substituents and the solvent used.
  • Impact of pH: The solubility may be affected by changes in pH, given the presence of acidic protons associated with the pyrimidine dione.

In summary, understanding the solubility of this compound requires consideration of both its structural components and the solvents in which it is being tested. As such, additional experimental data may be necessary to fully characterize its solubility properties.

Interesting facts

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

This compound is a fascinating member of the pyrimidine family, which is critical in many biological processes. Pyrimidines themselves serve as the structural basis for key biomolecules such as DNA and RNA, making this compound an intriguing subject of study.


Structural Features

The unique structure of this compound includes:

  • Substituated pyrimidine ring: The modification of both the 5 and 2 positions results in enhanced chemical properties.
  • Presence of sulfur: The sulfur atoms not only contribute to the compound's reactivity but also influence its biological activity.
  • Butyl and ethyl groups: These alkyl chains increase the compound's lipophilicity, potentially affecting its interaction with biological membranes.

Biological Relevance

Pyrimidine derivatives, such as this one, can exhibit:

  • Antimicrobial properties: Many compounds in this class have been researched for their effectiveness against various pathogens.
  • Anticancer activity: Some pyrimidine derivatives show promise in inhibiting tumor growth, making them valuable in cancer research.
  • Enzyme inhibition: Their ability to interact with specific enzymes can result in varied pharmacological effects.

Research Potential

This compound offers several avenues for further investigation:

  • Exploring its potential as a drug candidate in medicinal chemistry.
  • Investigating its mechanisms of action in biological systems.
  • Assessing its environmental impact and degradation pathways.

Understanding compounds like 5-(butylsulfanylmethyl)-5-ethyl-2-sulfanyl-1H-pyrimidine-4,6-dione is not just a matter of chemistry; it encompasses biochemistry, pharmacology, and environmental science, showcasing the interconnectedness of various scientific fields.