Sodium 5-ethyl-4,6-dioxo-5-phenyl-1H-pyrimidin-2-olate

Identification

Molecular formula

NaC₁₄H₁₁N₂O₃

CAS number

2082-77-9

IUPAC name

sodium;5-ethyl-4,6-dioxo-5-phenyl-1H-pyrimidin-2-olate

State

At room temperature, the compound is a solid.

Melting point (Celsius)

150.00

Melting point (Kelvin)

423.00

Boiling point (Celsius)

350.00

Boiling point (Kelvin)

623.00

General information

Molecular weight

284.27g/mol

Molar mass

284.2670g/mol

Density

1.3700g/cm³

Appearence

Sodium 5-ethyl-4,6-dioxo-5-phenyl-1H-pyrimidin-2-olate typically presents as a crystalline solid. The color can range depending on impurities and hydration state, but it is commonly seen as a white to off-white powder.

Comment on solubility

Solubility of Sodium; 5-ethyl-4,6-dioxo-5-phenyl-1H-pyrimidin-2-olate (NaC₁₄H₁₁N₂O₃)

The solubility of NaC₁₄H₁₁N₂O₃ can vary based on several factors, including temperature, pH, and the presence of other ions in the solution. Generally, sodium salts tend to exhibit good solubility in water, and this compound may follow a similar trend.

Factors Affecting Solubility

Temperature: Increased temperatures often enhance solubility. As the temperature rises, the kinetic energy increases and the solute molecules are more likely to overcome intermolecular forces.
pH Levels: The acidic or basic conditions of the solution can significantly influence the solubility of the compound. A more alkaline environment might improve the solubility of certain organic compounds.
Ionic Strength: The presence of other ions in solution can lead to common ion effects, which may either promote or inhibit solubility.

In conclusion, while NaC₁₄H₁₁N₂O₃ demonstrates promising solubility characteristics typical of sodium-based compounds, specific solubility tests are essential to provide detailed insights. "Every sodium compound tells a story of solubility." Understanding this aspect is crucial for applications in various fields such as pharmaceuticals, agriculture, and chemical synthesis.

Interesting facts

Exploring Sodium; 5-Ethyl-4,6-Dioxo-5-Phenyl-1H-Pyrimidin-2-Olate

Sodium; 5-ethyl-4,6-dioxo-5-phenyl-1H-pyrimidin-2-olate is a fascinating compound with unique properties and applications in the field of chemistry. This compound is part of the broader class of pyrimidine derivatives, which are essential components in biochemistry and pharmaceutical chemistry.

Key Characteristics:

Presence of Dioxo Groups: The compound features two carbonyl functional groups, which significantly influence its reactivity and biological activity.
Substituent Effects: The ethyl and phenyl groups attached to the pyrimidine ring enhance its lipophilicity, making it a potential candidate for studies involving drug formulation and delivery.
Biological Relevance: Pyrimidine derivatives are known to play crucial roles in pharmacology, with some compounds exhibiting antitumor and antiviral activities.

This compound exemplifies the intricate relationship between structure and function within chemical compounds. Its unique arrangement of atoms not only plays a vital role in its reactivity but also opens doors to various applications in the pharmaceutical industry.

Applications in Research:

Drug Development: Researchers are continually exploring the medicinal properties of pyrimidine derivatives for possible therapeutic applications.
Analytical Chemistry: Due to its distinct spectral properties, it may be utilized in developing analytical techniques for identifying similar compounds in biological studies.

In conclusion, sodium; 5-ethyl-4,6-dioxo-5-phenyl-1H-pyrimidin-2-olate is more than just a chemical formula; it represents the complex interaction of chemistry and biology, driving advancements in science and medicine.