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Thiobarbituric acid

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Identification
Molecular formula
C6H6N2OS
CAS number
504-17-6
IUPAC name
5-but-2-enyl-5-butyl-2-sulfanyl-1H-pyrimidine-4,6-dione
State
State

Thiobarbituric acid is typically solid at room temperature. It has a stable crystalline form and is handled and shipped as a solid material in laboratory and industrial settings.

Melting point (Celsius)
210.00
Melting point (Kelvin)
483.15
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
144.17g/mol
Molar mass
144.1650g/mol
Density
1.4788g/cm3
Appearence

Thiobarbituric acid appears as a white to off-white crystalline powder. It may have a mild odor and is typically solid at room temperature. The compound has a crystalline structure and is often used in laboratories for various chemical reactions and experiments.

Comment on solubility

Solubility of 5-but-2-enyl-5-butyl-2-sulfanyl-1H-pyrimidine-4,6-dione

The solubility of 5-but-2-enyl-5-butyl-2-sulfanyl-1H-pyrimidine-4,6-dione in various solvents can vary significantly due to its unique structural characteristics. Generally, solubility is influenced by several factors, which include:

  • Polarity: The presence of functional groups in the compound can affect its polarity, thus influencing solubility in polar or non-polar solvents.
  • Hydrogen bonding: If the compound can participate in hydrogen bonding, it might exhibit increased solubility in protic solvents.
  • Molecular weight: Higher molecular weight compounds tend to have lower solubility in many solvents due to reduced mobility.
  • Temperature: Solubility often increases with temperature, so experimenting at different temperatures might yield varying results.

In practical terms, while there may not be extensive literature specifically on the solubility of this compound, it is plausible that it shows better solubility in organic solvents like ethanol or dimethyl sulfoxide (DMSO), compared to water, due to the non-polar hydrocarbon chain and bulky structure.

Researchers should conduct solubility tests in various solvents to accurately determine the most suitable ones for this compound, as the molecular interactions can yield surprising results!

Interesting facts

Interesting Facts about 5-but-2-enyl-5-butyl-2-sulfanyl-1H-pyrimidine-4,6-dione

This compound, known as 5-but-2-enyl-5-butyl-2-sulfanyl-1H-pyrimidine-4,6-dione, is a fascinating member of the pyrimidine family, a class of organic compounds characterized by their six-membered ring structure containing nitrogen atoms. Here are some engaging insights into this intriguing compound:

  • Complex Structure: The compound features a pyrimidine ring with additional alkyl and sulfur groups, making it a unique structure that can have various chemical interactions and properties.
  • Potential Biological Activity: Compounds related to pyrimidine have been widely studied for their biological activities, including antiviral and anticancer properties. The presence of both sulfur and alkyl side chains may enhance its activity in medicinal chemistry.
  • Versatile Synthetic Routes: Chemists often explore diverse synthetic methods to create complex compounds like this one. These methods make it possible to modify the structure for desired properties, allowing for exploration in pharmaceuticals and other applications.
  • Reactivity: Due to the presence of double bonds (alkenes) in its structure, 5-but-2-enyl-5-butyl-2-sulfanyl-1H-pyrimidine-4,6-dione may undergo various chemical reactions such as electrophilic additions, making it a valuable intermediate in organic synthesis.
  • Research Opportunities: This compound could serve as a starting point for the development of new drugs and agrochemicals. Ongoing research in organic and medicinal chemistry continues to unveil potential applications of similar compounds.

In summary, 5-but-2-enyl-5-butyl-2-sulfanyl-1H-pyrimidine-4,6-dione is not just a chemical entity but a gateway to exploring new and promising areas in chemistry, bridging the gap between structure and biological activity.