Skip to main content

Notomelia

ADVERTISEMENT
Identification
Molecular formula
C14H8N4O6S
CAS number
151127-32-1
IUPAC name
6-(dihydroxyamino)-2,3-dioxo-benzo[f]quinoxaline-7-sulfonamide
State
State

At room temperature, this compound is a solid.

Melting point (Celsius)
276.00
Melting point (Kelvin)
549.15
Boiling point (Celsius)
420.00
Boiling point (Kelvin)
693.15
General information
Molecular weight
335.30g/mol
Molar mass
335.3100g/mol
Density
1.8500g/cm3
Appearence

The compound appears as a colorless crystalline solid. It is known for its distinct quinoxaline core, which contributes to its crystalline structure.

Comment on solubility

Solubility of 6-(dihydroxyamino)-2,3-dioxo-benzo[f]quinoxaline-7-sulfonamide

The solubility of 6-(dihydroxyamino)-2,3-dioxo-benzo[f]quinoxaline-7-sulfonamide (C14H8N4O6S) can be influenced by several factors, given its complex structure and functional groups. Here are some key points regarding its solubility:

  • Polarity: The presence of multiple hydroxyl (-OH) and sulfonamide (-SO₂NH₂) groups contribute to the **polarity** of the compound, which typically enhances solubility in polar solvents, such as water.
  • Hydrogen Bonding: The ability to form hydrogen bonds with water molecules might facilitate the dissolution process, making it more soluble in aqueous solutions.
  • pH Sensitivity: The solubility of sulfonamides often varies with pH. In more acidic or basic environments, the ionization of functional groups can significantly alter solubility.
  • Temperature Effects: As is often the case with many compounds, increasing the temperature may increase solubility due to enhanced molecular movement that overcomes intermolecular forces.

In summary, while specific experimental data on the solubility of this compound may vary, it's reasonable to anticipate moderate to high solubility in polar solvents, influenced by the factors discussed above. As always, consulting experimental studies will provide the most reliable solubility information for practical applications.

Interesting facts

Exploring 6-(Dihydroxyamino)-2,3-dioxo-benzo[f]quinoxaline-7-sulfonamide

This fascinating compound, with its complex structure, belongs to the class of sulfonamides and exhibits unique properties that make it a subject of interest in various fields such as medicinal chemistry and biochemistry. Here are some intriguing facts about this compound:

  • Biological Relevance: This compound has been studied for its potential therapeutic applications, particularly in anti-cancer and anti-inflammatory contexts. Its intricate structure allows for interactions at the molecular level that may lead to significant biological effects.
  • Mechanism of Action: Similar to other sulfonamides, this compound may work by inhibiting the synthesis of bacterial folate, a vital nutrient for microbial growth. This mechanism makes it an important compound in the development of antibacterial agents.
  • Research Opportunities: The presence of both amine and sulfonamide functional groups provides ample room for chemical modifications. Researchers are excited about the potential to synthesize derivatives with enhanced efficacy or reduced side effects.
  • Analytical Techniques: The complexity of this compound’s structure requires advanced techniques such as nuclear magnetic resonance (NMR) spectroscopy and mass spectrometry for structure elucidation and understanding its properties.
  • Environmental Impact: As researchers investigate the stability and degradation of sulfonamide compounds, understanding their environmental fate is crucial. This can help mitigate potential pollution issues associated with pharmaceutical compounds.

"In science, there are no shortcuts to truth." – Karl Popper This quote perfectly encapsulates the journey of exploring compounds like 6-(dihydroxyamino)-2,3-dioxo-benzo[f]quinoxaline-7-sulfonamide, where every study contributes to a more profound understanding of chemistry and its applications.

As new research emerges, the capabilities of this compound continue to pique interest, solidifying its place in the exploration of innovative treatments and therapies.