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Dihydropteridine

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Identification
Molecular formula
C6H5N5O2
CAS number
119-94-8
IUPAC name
2-amino-1,8-dihydropteridine-4,7-dione
State
State

At room temperature, Dihydropteridine is typically in a solid state.

Melting point (Celsius)
350.00
Melting point (Kelvin)
623.15
Boiling point (Celsius)
550.00
Boiling point (Kelvin)
823.15
General information
Molecular weight
177.17g/mol
Molar mass
177.1660g/mol
Density
1.4500g/cm3
Appearence

Dihydropteridine typically appears as a crystalline solid that may be colorless or pale yellow. It is not well characterized in terms of commercially available material appearance.

Comment on solubility

Solubility of 2-amino-1,8-dihydropteridine-4,7-dione

The solubility of 2-amino-1,8-dihydropteridine-4,7-dione is an intriguing topic that showcases the complex interactions governing the dissolution of chemical compounds. This particular compound, known for its unique structure, has various solubility characteristics influenced by environmental factors. Here are some key points regarding its solubility:

  • Polar vs. Nonpolar Solvents: 2-amino-1,8-dihydropteridine-4,7-dione exhibits better solubility in polar solvents due to the presence of amino groups, which facilitate hydrogen bonding.
  • pH Dependence: The solubility may vary with pH, as the ionization of the amino groups can change its solubility profile significantly.
  • Temperature Effects: As with many compounds, an increase in temperature generally leads to an increase in solubility, making it crucial to consider temperature when preparing solutions.

It is noted that this compound may not be highly soluble in nonpolar solvents due to its polar nature. The phrase “like dissolves like” serves as a reminder that the solubility of a compound often aligns with the polarity of the solvent used. Understanding these factors can be essential for chemists when utilizing 2-amino-1,8-dihydropteridine-4,7-dione in various experimental conditions.

Interesting facts

Interesting Facts about 2-Amino-1,8-dihydropteridine-4,7-dione

This intriguing compound, known as 2-amino-1,8-dihydropteridine-4,7-dione, is best recognized for its role as a precursor in various biochemical pathways and its relevance in medicinal chemistry. Here are some captivating insights:

  • Biosynthesis: This compound is a key intermediate in the biosynthesis of folate coenzymes, which are vital for DNA synthesis and repair.
  • Biological Importance: Folate derivatives are essential for cellular division, making this compound significant in the context of cellular metabolism.
  • Potential Therapeutic Applications: Research has investigated the role of dihydropteridine derivatives in various diseases, including cancer, since they may influence cellular growth and metabolic pathways.
  • Medical Relevance: Compounds like 2-amino-1,8-dihydropteridine-4,7-dione have been studied for their potential use in treating conditions associated with folate deficiency and are even explored for their neuroprotective effects.

Furthermore, the structure of 2-amino-1,8-dihydropteridine-4,7-dione incorporates a pteridine ring system, which is a fascinating aspect for chemists due to its variety of derivatives and reactions. This compound exemplifies how a simple alteration in chemical structure can lead to a broad spectrum of biological activity and application in pharmacology. As such, it underscores the intricate relationship between chemistry and biology.

In summary, 2-amino-1,8-dihydropteridine-4,7-dione is not merely a compound but a vital player in the world of biochemistry, paving the way for innovations in healthcare and therapeutic strategies.