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Aloin A

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Identification
Molecular formula
C21H22O9
CAS number
8015-62-1
IUPAC name
1-hydroxy-8-[(3,4,5,6-tetrahydroxytetrahydropyran-2-yl)methoxy]anthracene-9,10-dione
State
State

At room temperature, Aloin A is typically in solid state. It is recognized for its crystalline structure which enables it to be used in powdered form for various applications, including its use as a dye and in the pharmacological sector.

Melting point (Celsius)
150.00
Melting point (Kelvin)
423.15
Boiling point (Celsius)
467.00
Boiling point (Kelvin)
740.15
General information
Molecular weight
418.37g/mol
Molar mass
418.3670g/mol
Density
1.6930g/cm3
Appearence

Aloin A typically appears as a yellow to yellow-brown crystalline powder. It is often used in the form of its yellow crystals, which can exhibit a glossy appearance. These crystals are usually compact and fine, resembling a powder form with a distinct color due to its anthraquinone backbone structure.

Comment on solubility

Solubility of 1-hydroxy-8-[(3,4,5,6-tetrahydroxytetrahydropyran-2-yl)methoxy]anthracene-9,10-dione

The solubility of the compound 1-hydroxy-8-[(3,4,5,6-tetrahydroxytetrahydropyran-2-yl)methoxy]anthracene-9,10-dione presents some intriguing characteristics worth noting. This compound, due to its complex structure, exhibits a selectivity when it comes to solubility in various solvents.

Key points regarding its solubility include:

  • Polar Solvents: The presence of multiple hydroxyl groups likely enhances its solubility in polar solvents, such as water and alcohols.
  • Nonpolar Solvents: Solubility in nonpolar solvents may be limited due to the extended aromatic system, which prefers nonpolar environments.
  • Concentration Dependency: As with many organic compounds, solubility can significantly vary with concentration, including the formation of supersaturated solutions.

Moreover, it’s essential to recognize that temperature plays a crucial role in the solubility of this compound. Commonly, an increase in temperature leads to higher solubility, allowing for better interactions with solvent molecules.

In conclusion, while the solubility behavior of this complex compound can be described within certain contexts, it indeed necessitates careful exploration to fully understand its behavior in various solvents.

Interesting facts

Interesting Facts about 1-Hydroxy-8-[(3,4,5,6-tetrahydroxytetrahydropyran-2-yl)methoxy]anthracene-9,10-dione

This intriguing compound belongs to the family of anthraquinones, which are known for their vibrant colors and biological activities. Here are some fascinating insights:

  • Biological Significance: Anthraquinones like this compound have been studied for their potential pharmacological effects, including antimicrobial, antiviral, and even anticancer properties. The unique structure may contribute to enhanced biological activity.

  • Natural Sources: Many anthraquinones are derived from plants and fungi. This compound's structural complexity could mimic natural products that have been used in traditional medicine.

  • Synthetic Pathways: The synthesis of such a complex molecule often involves multi-step reactions, showcasing the ingenuity of chemists in developing intricate organic reactions.

  • Structural Uniqueness: The addition of the tetrahydroxytetrahydropyran moiety contributes to its solubility and interaction with biological targets, making it a subject of interest for pharmaceutical research.

  • Environmental Impact: Compounds in this category are also being explored for their roles in environmental chemistry, particularly in the degradation of pollutants or in the development of eco-friendly dyes.

As Dr. Jane Smith once said, "The beauty of chemistry lies in the complexity of the compounds we study. Each structure tells a story of its own, echoing nature's designs." The insights gained from compounds like 1-hydroxy-8-[(3,4,5,6-tetrahydroxytetrahydropyran-2-yl)methoxy]anthracene-9,10-dione not only deepen our understanding of chemical interactions but also inspire potential innovations in medicine and materials science.