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Sodium barbiturate

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Identification
Molecular formula
C5H3N2NaO4
CAS number
591-02-8
IUPAC name
sodium;2,4-dioxo-1H-pyrimidine-6-carboxylate
State
State

At room temperature, sodium barbiturate is typically in a solid state as a white crystalline powder.

Melting point (Celsius)
300.00
Melting point (Kelvin)
573.15
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
184.08g/mol
Molar mass
184.0800g/mol
Density
1.3500g/cm3
Appearence

Sodium barbiturate typically appears as a white crystalline powder. It is odorless and has a slightly bitter taste.

Comment on solubility

Solubility of Sodium; 2,4-Dioxo-1H-Pyrimidine-6-Carboxylate

Sodium; 2,4-dioxo-1H-pyrimidine-6-carboxylate, often represented in its ionic form, exhibits interesting solubility characteristics largely influenced by its molecular structure and the presence of ionic groups. Below are some key points regarding its solubility:

  • Ionic Nature: Being a sodium salt, it is more likely to be soluble in polar solvents such as water.
  • Influence of pH: The solubility can vary with pH levels; it tends to be more soluble in alkaline conditions due to the deprotonation of acidic groups.
  • Temperature Dependence: Higher temperatures generally increase solubility for many salts, and this compound is no exception.
  • Complex Formation: It might form complexes with metal ions or other solutes, potentially affecting its solubility in various solutions.

In general, one can expect sodium; 2,4-dioxo-1H-pyrimidine-6-carboxylate to be readily soluble in aqueous environments, making it useful in various chemical applications.

Interesting facts

Interesting Facts about Sodium; 2,4-Dioxo-1H-Pyrimidine-6-Carboxylate

Sodium; 2,4-dioxo-1H-pyrimidine-6-carboxylate, commonly referred to in the scientific community as a derivative of pyrimidine, holds significant importance in various fields of study. Here are some noteworthy facts:

  • Biochemical Role: This compound serves as an intermediate in the synthesis of nucleotides, which are the building blocks of RNA and DNA. Its structure supports various enzymatic reactions vital for cellular processes.
  • Pharmaceutical Applications: Compounds containing the pyrimidine structure have been extensively studied for their potential in developing drugs, particularly in treating viral infections and certain types of cancer.
  • Versatile Reactivity: The presence of multiple functional groups allows for a range of chemical reactions, making it a versatile compound in organic synthesis. It can be used in the creation of various heterocycles.
  • Research Interest: Scientists are continuously exploring the properties and reactivity of this compound. Research indicates that modifications to its structure can lead to enhanced pharmacological activities.
  • Educational Value: This compound is often included in academic curricula focused on organic chemistry, particularly in studying reaction mechanisms and the formation of heterocyclic compounds.

As a student or a scientist delving into the world of organic compounds, understanding sodium; 2,4-dioxo-1H-pyrimidine-6-carboxylate unveils a fascinating interplay of chemistry and biology. The potential implications of this compound are vast and varied, making it an exciting area of research and study.