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Sodium barbitone

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Identification
Molecular formula
C10H11N2NaO3
CAS number
57-44-3
IUPAC name
sodium;5-butyl-1-cyclohexyl-4,6-dioxo-pyrimidin-2-olate
State
State

Sodium barbitone exists as a solid at room temperature.

Melting point (Celsius)
215.00
Melting point (Kelvin)
488.15
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
246.20g/mol
Molar mass
246.2610g/mol
Density
1.2100g/cm3
Appearence

Sodium barbitone, also known as sodium barbital, typically appears as a white, crystalline powder. It is odorless and may have a slightly bitter taste. The compound is readily soluble in water, forming clear solutions.

Comment on solubility

Solubility of Sodium; 5-butyl-1-cyclohexyl-4,6-dioxo-pyrimidin-2-olate

The solubility of sodium; 5-butyl-1-cyclohexyl-4,6-dioxo-pyrimidin-2-olate (commonly referred to as sodium butylcyclohexylpyrimidinedione) can be intriguing due to its unique chemical structure. Understanding the solubility of this compound is crucial for its applications in various fields, such as pharmaceuticals and materials science.

Factors Influencing Solubility:

  • Polarity: The presence of a sodium ion enhances solubility in polar solvents, while the cyclohexyl and butyl groups may impart hydrophobic characteristics, thus affecting the solubility in non-polar solvents.
  • Temperature: Generally, an increase in temperature can enhance the solubility of solids in liquids, but this is subject to the specific interactions of the compound involved.
  • pH of the Solution: As a sodium salt, the solubility may vary significantly with changes in pH, impacting how the compound interacts with water.

In summary, sodium; 5-butyl-1-cyclohexyl-4,6-dioxo-pyrimidin-2-olate's solubility is influenced by factors such as polarity, temperature, and pH.
Understanding these factors can aid in predicting the behavior of the compound in various environments, making it essential for researchers and developers alike.

Interesting facts

Interesting Facts about Sodium; 5-butyl-1-cyclohexyl-4,6-dioxo-pyrimidin-2-olate

This intriguing compound is a derivative of pyrimidine, a class of molecules that plays a crucial role in biochemistry and pharmacology. Here are some compelling facts that highlight its significance:

  • Pyrimidine Base: The compound features a pyrimidine ring, which is essential in the structure of nucleic acids like DNA and RNA. This highlights its importance in genetic information transfer.
  • Biological Applications: Compounds with similar structures are often investigated for their biological activities, including their potential to act as enzyme inhibitors or therapeutic agents.
  • Sodium Component: The presence of sodium in this compound may enhance its solubility and bioavailability, making it interesting for pharmaceutical applications.
  • Cyclohexyl Group: The cyclohexyl moiety contributes to the compound's hydrophobic characteristics, which can alter interactions with biological membranes.
  • Oxo Groups: The 4,6-dioxo groups provide sites for hydrogen bonding and can influence the compound's reactivity and stability.

The unique combination of functional groups in sodium; 5-butyl-1-cyclohexyl-4,6-dioxo-pyrimidin-2-olate suggests potential avenues for research in areas like cancer treatment or antibiotic development. Its architectural complexity is a testament to the diversity found in chemical compounds, reminding us of the endless possibilities within the realm of chemistry.

As the renowned chemist Linus Pauling once said, "The best way to have a good idea is to have a lot of ideas." This compound embodies the spirit of exploration and innovation in the field of chemistry, encouraging further investigation into its properties and applications.