Sodium barbital
- 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
- Molecular Weight
- 238.25g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.2500g/cm3
Identification
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!