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Melianthin

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Identification
Molecular formula
C15H18O4
CAS number
1948-95-2
IUPAC name
(3aS,6S,6aR,9aS,9bR)-6a-hydroxy-6,9a-dimethyl-3-methylene-4,5,6,9b-tetrahydro-3aH-azuleno[8,7-b]furan-2,9-dione
State
State

At room temperature, the compound exists in a solid state, often as crystalline powder.

Melting point (Celsius)
78.00
Melting point (Kelvin)
351.15
Boiling point (Celsius)
350.00
Boiling point (Kelvin)
623.15
General information
Molecular weight
282.30g/mol
Molar mass
282.3030g/mol
Density
1.3400g/cm3
Appearence

The compound is typically a solid with a crystalline appearance. It may appear as a white to off-white crystalline powder under normal conditions.

Comment on solubility

Solubility of (3aS,6S,6aR,9aS,9bR)-6a-hydroxy-6,9a-dimethyl-3-methylene-4,5,6,9b-tetrahydro-3aH-azuleno[8,7-b]furan-2,9-dione

The solubility of (3aS,6S,6aR,9aS,9bR)-6a-hydroxy-6,9a-dimethyl-3-methylene-4,5,6,9b-tetrahydro-3aH-azuleno[8,7-b]furan-2,9-dione can be influenced by various factors including its molecular structure and the presence of functional groups. Understanding the solubility characteristics of this compound is essential for its application in various fields.

Key Points Regarding Solubility:

  • Polar vs. Nonpolar Environment: The compound contains hydroxyl groups which could enhance its solubility in polar solvents, while the hydrocarbon-like structure may limit solubility in purely nonpolar solvents.
  • Temperature Dependence: Solubility may increase with temperature, allowing better dissolution in solvents when heated.
  • pH Influence: If the compound can ionize, the solubility could be affected by the acidity or basicity of the solvent.
  • Concentration Effects: At higher concentrations, solubility may decrease due to potential saturation.

In conclusion, while the detailed solubility profile can be complex and dependent on specific conditions, it is crucial to consider the factors mentioned above when evaluating the solubility of (3aS,6S,6aR,9aS,9bR)-6a-hydroxy-6,9a-dimethyl-3-methylene-4,5,6,9b-tetrahydro-3aH-azuleno[8,7-b]furan-2,9-dione in practical applications.

Interesting facts

Interesting Facts about (3aS,6S,6aR,9aS,9bR)-6a-hydroxy-6,9a-dimethyl-3-methylene-4,5,6,9b-tetrahydro-3aH-azuleno[8,7-b]furan-2,9-dione

The compound known by the intricate name (3aS,6S,6aR,9aS,9bR)-6a-hydroxy-6,9a-dimethyl-3-methylene-4,5,6,9b-tetrahydro-3aH-azuleno[8,7-b]furan-2,9-dione is a fascinating example of organic chemistry at its best. Its complex structure offers a treasure trove of insights for both researchers and students alike.

Key Features:

  • Unique Structure: This compound features a multi-ring system, typical of azulene derivatives, which is known for its unusual properties compared to typical hydrocarbons.
  • Hydroxy Group: The presence of a hydroxy group introduces *functional versatility*, allowing for potential applications in various chemical reactions and interactions.
  • Dimethyl Substituents: The dimethyl groups can enhance its *lipophilicity*, impacting its behavior in biological systems.
  • Tetrahydro Structure: The tetrahydro configuration suggests that this molecule may possess unique *conformational characteristics*, which can influence its reactivity and interactions.

Applications and Potential:

Despite its complex structure, research into azulene derivatives has revealed several potential applications, including:

  • Antioxidant Properties: Compounds in the azulene family often exhibit antioxidant activity, which is crucial in mitigating oxidative stress in biological systems.
  • Biological Interest: There is ongoing research into the therapeutic potential of these compounds, particularly in the fields of medicine and pharmacology.
  • Chemical Synthesis: The compound can be a useful intermediate in organic synthesis, providing a pathway to more complex molecules.

As chemists continue to explore the vast potential of compounds like this, they not only expand our understanding of organic chemistry but also pave the way for innovative solutions in various fields, from materials science to pharmaceuticals.

Synonyms
Hymenin
Epiparthenin
20555-04-8
(3aS,6S,6aR,9aS,9bR)-6a-hydroxy-6,9a-dimethyl-3-methylidene-4,5,6,9b-tetrahydro-3aH-azuleno[8,7-b]furan-2,9-dione
1beta,10alphaH-Ambrosa-2,11(13)-dien-12-oic acid, 1,6beta-dihydroxy-4-oxo-, gamma-lactone
Azuleno(4,5-b)furan-2,9-dione, 3,3a,4,5,6,6a,9a,9b-octahydro-6a-hydroxy-6,9a-dimethyl-3-methylene-, (3aS,6S,6aR,9aS,9bR)-
Azuleno(4,5-b)furan-2,9-dione, 3,3a,4,5,6,6a,9a,9b-octahydro-6a-hydroxy-6,9a-dimethyl-3-methylene-, (3aS-(3aalpha,6beta,6abeta,9abeta,9balpha))-
(3aS,6S,6aR,9aS,9bR)-6a-hydroxy-6,9a-dimethyl-3-methylidene-4,5,6,9b-tetrahydro-3aH-azuleno(8,7-b)furan-2,9-dione
CHEMBL312004
NS00094025