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Benzo[1,2-c:3,4-c']diquinoline-6,12-dione

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Identification
Molecular formula
C34H20N2O6
CAS number
22750-19-4
IUPAC name
N-[8-[(8-benzamido-9,10-dioxo-1-anthryl)amino]-9,10-dioxo-1-anthryl]benzamide
State
State

At room temperature, the compound is generally found in a solid state, specifically as a crystalline powder.

Melting point (Celsius)
289.00
Melting point (Kelvin)
562.00
Boiling point (Celsius)
553.00
Boiling point (Kelvin)
826.00
General information
Molecular weight
514.51g/mol
Molar mass
514.5100g/mol
Density
1.2800g/cm3
Appearence

The compound is typically a colorful powder ranging in hues from light yellow to orange-red, depending on its exact formulation and purity.

Comment on solubility

Solubility of N-[8-[(8-benzamido-9,10-dioxo-1-anthryl)amino]-9,10-dioxo-1-anthryl]benzamide

N-[8-[(8-benzamido-9,10-dioxo-1-anthryl)amino]-9,10-dioxo-1-anthryl]benzamide is a complex organic compound characterized by its intricate structure. Understanding its solubility is crucial for its applications in various chemical and biological processes.

Key Factors Affecting Solubility:

  • Polarity: The presence of multiple functional groups in the molecule influences its ability to dissolve in polar or non-polar solvents.
  • Molecular Size: Larger molecules often have lower solubility due to steric hindrance and decreased interaction with solvent molecules.
  • Hydrogen Bonding: The ability to form hydrogen bonds can enhance solubility in polar solvents, while lack of such interactions may lead to decreased solubility.

Due to the structural complexity, one might observe that:

  • The compound may exhibit low solubility in water, given its extensive aromatic components.
  • In organic solvents such as DMSO or acetone, solubility may increase due to the hydrophobic interactions and favorable solvent-solute interactions.

In conclusion, the solubility of N-[8-[(8-benzamido-9,10-dioxo-1-anthryl)amino]-9,10-dioxo-1-anthryl]benzamide will vary significantly depending on the solvent used and the conditions of the solution process. Understanding these dynamics can help in appropriately choosing solvents for dissolution and application in further chemical reactions.

Interesting facts

Interesting Facts about N-[8-[(8-benzamido-9,10-dioxo-1-anthryl)amino]-9,10-dioxo-1-anthryl]benzamide

N-[8-[(8-benzamido-9,10-dioxo-1-anthryl)amino]-9,10-dioxo-1-anthryl]benzamide is a member of the anthraquinone family, known for its significant roles in various fields of chemistry and biochemistry. This compound showcases a fascinating structure that contributes to its unique properties and potential applications.

Chemical Structure and Properties

  • Anthraquinone Framework: The compound includes an anthraquinone core, which is notable for its strong and vibrant color properties, often leading to its use as a dye in textile industries.
  • Dual Dioxo Groups: The presence of two dioxo functional groups enhances the reactivity and interaction with biological systems, making it a subject of interest in pharmacological research.
  • Benzamide Moiety: The addition of the benzamide group not only influences solubility and stability but also contributes to its biological activity.

Biological Relevance

This compound has attracted attention due to its potential applications in medicinal chemistry. Some significant aspects include:

  • Investigated for antitumor activities, utilizing its ability to interact with cellular pathways effectively.
  • Studied for its role in photodynamic therapy, where light-activated compounds are used to target and destroy cancer cells.
  • The ability to act as a fluorescent probe for biological imaging, assisting researchers in tracking molecular interactions in living systems.

Research and Applications

Research continues to explore the various applications of this compound in different domains. Future prospects include:

  • Development of targeted drug delivery systems using the compound's unique structure to direct therapies to specific tissues.
  • Studies aimed at fine-tuning its photophysical properties to improve efficacy in therapeutic applications.
  • Potential use in creating sensors for detecting specific biomolecules, leveraging its structural properties.

In conclusion, N-[8-[(8-benzamido-9,10-dioxo-1-anthryl)amino]-9,10-dioxo-1-anthryl]benzamide is a compelling compound that bridges the gap between fundamental chemistry and practical application in biomedicine, illustrating the profound impact that chemical structures can have on function and utility.