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Dihydropyrazolopyrimidinedione

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Identification
Molecular formula
C5H4N4O2
CAS number
288-32-4
IUPAC name
1,2-dihydropyrazolo[3,4-d]pyrimidine-4,6-dione
State
State

This compound is a solid at room temperature.

Melting point (Celsius)
230.00
Melting point (Kelvin)
503.15
Boiling point (Celsius)
295.00
Boiling point (Kelvin)
568.15
General information
Molecular weight
139.12g/mol
Molar mass
139.1220g/mol
Density
1.5240g/cm3
Appearence

1,2-Dihydropyrazolo[3,4-d]pyrimidine-4,6-dione typically presents as a white to off-white crystalline solid.

Comment on solubility

Solubility of 1,2-Dihydropyrazolo[3,4-d]pyrimidine-4,6-dione

The solubility of the compound 1,2-dihydropyrazolo[3,4-d]pyrimidine-4,6-dione (C5H4N4O2) can often be influenced by its unique structure and the presence of functional groups. Here are some key points to consider regarding its solubility:

  • Polarity: The compound features various nitrogen and oxygen atoms that can contribute to its polarity. This typically enhances its solubility in polar solvents.
  • Interactions: Hydrogen bonding capabilities from the carbonyl groups may facilitate solubility in hydrogen-bonding solvents like water and alcohols.
  • Temperature Sensitivity: The solubility could vary significantly with temperature; thus, it is important to evaluate solubility at different temperatures.
  • Solvent Type: Solubility may differ in various solvents. For example, it might be more soluble in dimethyl sulfoxide (DMSO) compared to non-polar solvents.

In summary, the solubility of 1,2-dihydropyrazolo[3,4-d]pyrimidine-4,6-dione highlights the importance of molecular structure and solvent interactions. It’s crucial to carry out empirical testing to determine the precise solubility under various conditions.

Interesting facts

Interesting Facts about 1,2-Dihydropyrazolo[3,4-d]pyrimidine-4,6-dione

1,2-Dihydropyrazolo[3,4-d]pyrimidine-4,6-dione is a fascinating compound that belongs to the family of pyrazolo-pyrimidines. Here are some intriguing insights:

  • Key Structure: The presence of the pyrazole and pyrimidine rings in its structure showcases its complexity and versatility, making it an interesting subject of study in organic chemistry.
  • Potential Biological Activity: Compounds in the pyrazolo-pyrimidine class have garnered interest for their potential therapeutic applications, including anti-inflammatory and anticancer properties. Reports suggest that derivatives of this compound may interact with various biological targets.
  • Synthetic Routes: Scientists have developed various synthetic pathways to generate this compound, highlighting its utility in organic synthesis. These routes often involve multi-step processes that can introduce various functional groups.
  • Research Applications: Ongoing research may further explore this compound's role in medicinal chemistry, especially as a lead compound for drug development. Its intriguing scaffolding allows chemists to modify and create new derivatives.
  • Future Prospects: With advances in chemical research, this compound may play a vital role not only in pharmaceuticals but also in agrochemicals and materials science. The potential is limitless!

Overall, 1,2-dihydropyrazolo[3,4-d]pyrimidine-4,6-dione represents a notable example of how intricate organic compounds can lead to significant advancements in various scientific fields. As researchers continue to explore its properties, the excitement around such compounds only deepens.