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Dinitroquinoxaline

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Identification
Molecular formula
C8H2N4O6
CAS number
2168-92-9
IUPAC name
6,7-dinitroquinoxaline-2,3-dione
State
State

At room temperature, 6,7-dinitroquinoxaline-2,3-dione is a solid. It is generally stable under normal conditions but should be handled with care due to its potentially explosive nature when in pure form, especially in powdered form.

Melting point (Celsius)
264.00
Melting point (Kelvin)
537.15
Boiling point (Celsius)
287.00
Boiling point (Kelvin)
560.15
General information
Molecular weight
236.12g/mol
Molar mass
236.1450g/mol
Density
1.6500g/cm3
Appearence

The compound typically appears as a crystalline solid, often with a pale yellow to tan coloration. It may exist in powdered form and can have a somewhat gritty texture depending on the sample.

Comment on solubility

Solubility of 6,7-dinitroquinoxaline-2,3-dione

6,7-Dinitroquinoxaline-2,3-dione, with the chemical formula C8H2N4O6, exhibits specific solubility characteristics that are noteworthy in the field of chemistry. Understanding the solubility of this compound can significantly influence its application and usability. Here are some essential points regarding its solubility:

  • Solvent Dependence: The solubility of 6,7-dinitroquinoxaline-2,3-dione primarily varies with the type of solvent used. It tends to be more soluble in polar solvents.
  • Temperature Effects: Generally, increasing the temperature can enhance solubility, making it imperative to consider temperature conditions during dissolution processes.
  • pH Influence: The pH of the solvent may play a crucial role in solubility, as acidic or basic conditions can affect the ionic form of the compound.
  • Practical Applications: Due to its limited solubility in non-polar solvents, the compound is typically utilized in specialized applications where polar solvents are the medium of choice.

As a conclusion, one might say that the solubility profile of 6,7-dinitroquinoxaline-2,3-dione is not just a simple characteristic but a vital aspect that dictates its behavior in various chemical environments, ultimately influencing its practical application in scientific research and industry.

Interesting facts

Interesting Facts about 6,7-Dinitroquinoxaline-2,3-dione

6,7-Dinitroquinoxaline-2,3-dione is a fascinating compound extensively studied in the field of biochemistry and pharmacology. Here are some noteworthy points:

  • Chemical Structure: This compound belongs to the quinoxaline family, characterized by a fused aromatic ring structure. The presence of electron-withdrawing nitro (-NO2) groups significantly impacts its chemical reactivity and biological activity.
  • Biological Activity: It is known for its role as a potent inhibitor of certain enzymes and receptors. Research shows that derivatives of this compound exhibit neuroprotective effects and potential applications in treating neurological disorders.
  • Research Applications: Scientists often utilize 6,7-dinitroquinoxaline-2,3-dione in neuropharmacological studies. For example, it acts as an antagonist for specific receptors, making it instrumental in dissecting neurotransmission pathways.
  • Toxicology: Like many nitro compounds, it is vital to handle this chemical with care due to its potential toxic effects. Investigations into its safety profile reveal important considerations for laboratory practices.
  • Historical Significance: The compound has contributed to various scientific advancements, particularly in understanding the mechanisms of synaptic transmission in the brain. Its study has uncovered important insights into how neurotransmitters affect cognitive functions.

Overall, 6,7-dinitroquinoxaline-2,3-dione exemplifies the intersection of chemistry and biology, highlighting the power of small molecules in influencing complex biological systems. As research continues, the potential for new therapeutic applications remains promising.

Synonyms
6,7-Dinitro-2,3-quinoxalinedione
114828-89-6
DTXSID50274395
DNQ
SCHEMBL157744
BDBM82560
DTXCID20225874
NSC_3140
CAS_2379-57-9
Q4386525