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Sodium barbital

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Identification
Molecular formula
C12H15N2NaO3
CAS number
103-60-6
IUPAC name
sodium;5-allyl-5-cyclohex-2-en-1-yl-6-oxo-2-sulfanyl-pyrimidin-4-olate
State
State

At room temperature, sodium barbital is typically found in a solid state. It is a crystalline powder.

Melting point (Celsius)
300.00
Melting point (Kelvin)
573.00
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
238.25g/mol
Molar mass
238.2500g/mol
Density
1.2500g/cm3
Appearence

Sodium barbital typically appears as a white crystalline powder.

Comment on solubility

Solubility of Sodium; 5-allyl-5-cyclohex-2-en-1-yl-6-oxo-2-sulfanyl-pyrimidin-4-olate

The solubility of sodium; 5-allyl-5-cyclohex-2-en-1-yl-6-oxo-2-sulfanyl-pyrimidin-4-olate can be influenced by various factors, including its molecular structure and interactions with solvents. Here are some key points to consider:

  • Nature of the Compound: The presence of both polar and nonpolar groups within this compound suggests possible solubility in a range of solvents.
  • Solvent Polarity: It is likely to be more soluble in polar solvents (such as water) due to the sulfanyl and pyrimidinyl functionalities, which can form hydrogen bonds.
  • Temperature Effects: As with many organic compounds, increased temperature may enhance solubility, allowing for greater molecular interactions.
  • Protonation State: In an aqueous environment, it may exist in different protonation states, which could further influence its solubility profile.

In summary, the solubility of this compound is a complex interplay of its chemical nature and solvent environment. While specific solubility data may be required for precise applications, understanding the above parameters can provide valuable insights into its behavior in various media.

Interesting facts

Interesting Facts about Sodium; 5-allyl-5-cyclohex-2-en-1-yl-6-oxo-2-sulfanyl-pyrimidin-4-olate

The compound Sodium; 5-allyl-5-cyclohex-2-en-1-yl-6-oxo-2-sulfanyl-pyrimidin-4-olate is a fascinating example of a hybrid molecule that showcases the interplay of various functional groups. Here are some intriguing points about this compound:

  • Versatile Applications: This compound may have potential applications in the fields of pharmaceuticals and agrochemicals due to its unique structural features, including the pyrimidine and thiol groups.
  • Sulfur Chemistry: The presence of the sulfanyl group not only enhances the chemical reactivity but also opens doors for synthesizing thioesters, thioethers, and other important derivatives.
  • Pyrimidin-4-olate Moiety: This structure is often associated with biological activity, and compounds containing pyrimidine rings are known for their ability to inhibit various enzymes, making them significant in drug discovery.
  • Allyl Group Dynamics: The allyl substituent contributes to the reactivity of the compound, potentially undergoing various reactions such as Michael additions or polymerization.

As a student delving into the complexities of organic chemistry, understanding the mechanisms behind the reactivity and synthesis of this compound could provide valuable insights into modern material science and medicinal chemistry. "Chemistry is like a big puzzle. Every compound is a piece that helps us complete the picture of molecular interactions and applications." Embrace the challenge and explore the wonders of such intricate compounds!