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Dihydropteridine

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Identification
Molecular formula
C6H6N4O2
CAS number
2748-00-3
IUPAC name
2-amino-1,5-dihydropteridine-4,6-dione
State
State

Dihydropteridine is typically a solid under standard conditions, as inferred from its structure and common properties of similar nitrogen-heterocyclic compounds.

Melting point (Celsius)
0.00
Melting point (Kelvin)
0.00
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
163.14g/mol
Molar mass
163.1440g/mol
Density
0.0000g/cm3
Appearence

The appearance of dihydropteridine is not well-documented in standard chemical literature, indicating it may not have a distinct or noteworthy appearance outside of specific laboratory or industrial contexts.

Comment on solubility

Solubility of 2-amino-1,5-dihydropteridine-4,6-dione

The solubility of 2-amino-1,5-dihydropteridine-4,6-dione (C6H6N4O2) can be quite intriguing, especially given its structural features. Here are some important points regarding its solubility:

  • Solvent Dependence: This compound is expected to show variable solubility in different solvents, being more soluble in polar solvents.
  • Hydrogen Bonding: The presence of amino and carbonyl groups allows for the formation of hydrogen bonds, contributing to its solubility in aqueous environments.
  • Temperature Effects: As with many organic compounds, the solubility may increase with a rise in temperature, making it more soluble at elevated temperatures.
  • pH Influence: The solubility may also be affected by pH levels; in more acidic or basic conditions, ionization can enhance solubility.

In conclusion, while specific quantitative solubility data might vary, understanding the factors affecting the solubility of 2-amino-1,5-dihydropteridine-4,6-dione provides insight into its behavior in various chemical environments. "A compound's solubility is not just a number; it's a dance of interactions!"

Interesting facts

Facts About 2-Amino-1,5-Dihydropteridine-4,6-Dione

2-Amino-1,5-dihydropteridine-4,6-dione is an intriguing compound that plays a vital role in various biochemical processes. Here are some fascinating facts about this compound:

  • Biochemical Significance: This compound is a crucial intermediate in the biosynthesis of folate derivatives, which are essential for DNA synthesis and cellular metabolism.
  • Enzymatic Activity: It serves as a substrate for several enzymes, particularly dihydropteridine reductase, influencing neurotransmitter synthesis and metabolism.
  • Medical Relevance: Research has shown that modified derivatives of this compound can have potential therapeutic applications, especially in treating folate-related disorders.
  • Structural Insights: The unique structure of this pteridine derivative allows it to interact with various biological molecules, further enriching its functional importance in living organisms.
  • Versatility: Its ability to shuttle between different oxidation states makes it a versatile compound in redox reactions within biological systems.

In summary, 2-amino-1,5-dihydropteridine-4,6-dione is not just a mere chemical intermediary; it is a pivotal player in the intricate web of life, showcasing how a seemingly simple structure can have profound implications in biochemistry and medicine.