Sodium 5-ethyl-4,6-dioxo-5-phenyl-1H-pyrimidin-2-olate
- Molecular formula
- NaC14H11N2O3
- CAS Number
- 2082-77-9
- IUPAC Name
- sodium;5-ethyl-4,6-dioxo-5-phenyl-1H-pyrimidin-2-olate
- Molecular Weight
- 284.27g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.3700g/cm3
Identification
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.