Pramepexole-praseodymium complex | Solubility of Things

Identification

Molecular formula

C₁₂H₁₅N₄Pr

IUPAC name

(2-amino-5a,7,8,9,9a,10-hexahydro-5H-pyrido[2,3-g]quinazolin-6-yl)azanide;praseodymium

State

At room temperature, this compound is in a solid state.

Melting point (Celsius)

150.00

Melting point (Kelvin)

423.15

Boiling point (Celsius)

230.00

Boiling point (Kelvin)

503.15

General information

Molecular weight

450.35g/mol

Molar mass

450.3450g/mol

Density

0.9000g/cm³

Appearence

This compound appears as a crystalline solid. The color may range from off-white to light pink depending on its purity and the presence of praseodymium, which itself is a silvery-white metal.

Comment on solubility

Solubility of (2-amino-5a,7,8,9,9a,10-hexahydro-5H-pyrido[2,3-g]quinazolin-6-yl)azanide;praseodymium

The solubility of the compound (2-amino-5a,7,8,9,9a,10-hexahydro-5H-pyrido[2,3-g]quinazolin-6-yl)azanide;praseodymium (C₁₂H₁₅N₄Pr) can be quite complex due to its multifaceted structure. Here are some key points to consider regarding its solubility:

Polarity Influences: This compound contains both polar and nonpolar characteristics which can result in varying solubility in different solvents.
Solvent Compatibility: It may exhibit increased solubility in polar solvents such as water, especially given the presence of amino groups that can form hydrogen bonds.
Metal Interaction: The presence of praseodymium can affect solubility, as its ionic nature might enhance solubility in certain ionic media.
Temperature Effects: Like many compounds, solubility can increase with temperature; thus, understanding the phase behavior at different temperatures is essential for practical applications.

In conclusion, the specific solubility behavior of this compound will ultimately depend on a variety of factors, including temperature, solvent type, and the interactions of its molecular structure with solvent molecules. As with many complex organic-metallic compounds, thorough experimental analysis is often required to fully characterize solubility in different mediums.

Interesting facts

Exploring (2-amino-5a,7,8,9,9a,10-hexahydro-5H-pyrido[2,3-g]quinazolin-6-yl)azanide;praseodymium

This fascinating compound, featuring both organic and metallic components, showcases the intriguing intersection of organic chemistry and materials science. With an organic moiety defined by a complex pyridoquinazoline structure attached to a praseodymium (Pr) moiety, it opens up a world of possibilities in various applications. Here are some interesting aspects worth noting:

Hybrid Nature: The combination of a nitrogen-rich organic compound with the rare earth element praseodymium grants this material unique properties, such as enhanced catalytic abilities and potentially interesting optical characteristics.
Biological Potential: Compounds with similar structural frameworks have been investigated for their potential biological activities, suggesting that this compound may exhibit interesting pharmacological properties.
Lanthanide Applications: As a member of the lanthanide series, praseodymium-based compounds are celebrated for their applications in magnets, phosphors, and as catalysts in various industrial processes.
Synthetic Routes: The synthesis of such compounds often includes complex multi-step reactions, showcasing the creativity and ingenuity required in modern organic synthesis and coordination chemistry.
Research Opportunities: The unique properties of this compound make it a candidate for research in materials science, especially in the design of new advanced materials and pharmaceuticals.

In conclusion, the study of (2-amino-5a,7,8,9,9a,10-hexahydro-5H-pyrido[2,3-g]quinazolin-6-yl)azanide;praseodymium not only reveals insights into the world of coordination compounds but also holds promise for advancements in both chemistry and materials research. As we continue to explore its properties and potential applications, this compound stands as a testament to the beauty and complexity of chemical science.