Skip to main content

N-Nitrosofenozon

ADVERTISEMENT
Identification
Molecular formula
C12H13N3O3
CAS number
15677-87-5
IUPAC name
5-(dihydroxyamino)-3-nitroso-6,7,8,9-tetrahydrobenzo[g]indol-2-one
State
State

At room temperature, this compound is typically found in a solid state, with a stable crystalline form.

Melting point (Celsius)
224.00
Melting point (Kelvin)
497.15
Boiling point (Celsius)
504.00
Boiling point (Kelvin)
777.15
General information
Molecular weight
247.25g/mol
Molar mass
42.0410g/mol
Density
1.4700g/cm3
Appearence

The compound typically appears as a crystalline solid that can vary in color, usually white or yellowish, depending on the specific sample and purity.

Comment on solubility

Solubility of 5-(dihydroxyamino)-3-nitroso-6,7,8,9-tetrahydrobenzo[g]indol-2-one (C12H13N3O3)

The solubility of 5-(dihydroxyamino)-3-nitroso-6,7,8,9-tetrahydrobenzo[g]indol-2-one in various solvents can provide important insights into its potential applications and reactivity. Understanding how this compound interacts with solvents is crucial for both laboratory handling and formulation. Here are some key factors influencing its solubility:

  • Polar versus Nonpolar Solvents: The presence of hydroxyl groups (-OH) often enhances solubility in polar solvents such as water, while the overall structure may limit solubility in nonpolar solvents.
  • Hydrogen Bonding: The ability of the dihydroxyamino and nitroso functional groups to form hydrogen bonds may significantly increase solubility in aqueous solutions.
  • pH Influence: The solubility might vary with the pH of the solution, particularly as the compound may exist in different ionic forms under varying pH conditions.
  • Temperature Dependence: Like many organic compounds, increasing the temperature often increases solubility, allowing for greater dissolution rates.

In summary, while specific experimental data on the solubility of this compound may be limited, its structural features suggest that it has the potential for decent solubility in polar, protic solvents, particularly under varying conditions. As with many organic molecules, the *interplay of its functional groups* and the *solvent environment* is key to predicting its behavior in solution.

Interesting facts

Interesting Facts about 5-(Dihydroxyamino)-3-nitroso-6,7,8,9-tetrahydrobenzo[g]indol-2-one

This intriguing compound, often referred to as a derivatives of the indole family, offers numerous fascinating insights for both chemists and pharmacologists. Here are some key points to consider:

  • Structural Diversity: The compound exhibits complex structural characteristics, incorporating a tetrahydrobenzo[g]indole framework, which contributes to its unique reactivity and biological properties.
  • Functional Groups: It contains both a nitroso group and hydroxylamine functionality, which can influence the compound's interaction with biological molecules and its potential applications in medicinal chemistry.
  • Biological Importance: Compounds with similar structures have been studied for their roles in various biological processes, including their effects on nitric oxide synthase and cell signaling pathways.
  • Potential Applications: The presence of nitrogen and oxygen in its structure may grant the compound antioxidant properties, making it of interest in the study of diseases related to oxidative stress.
  • Research Opportunities: The versatility of this compound invites further investigation, particularly in developing new pharmaceuticals or in studying its role as a potential biomarker.

Quote from a chemist: "Understanding the nuances of such complex molecules can reveal pathways to innovations in treatment and prevention of various health conditions."

Overall, the study of 5-(dihydroxyamino)-3-nitroso-6,7,8,9-tetrahydrobenzo[g]indol-2-one can not only enhance our comprehension of indole derivatives but also pave the way for future discoveries in the realms of chemistry and medicine.