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Endiandric acid C

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Identification
Molecular formula
C20H22O5
CAS number
118455-84-2
IUPAC name
(4S)-15,17-dihydroxy-4-methyl-3-oxabicyclo[12.4.0]octadeca-1(14),12,15,17-tetraene-2,8-dione
State
State

Endiandric acid C is typically found in a solid state at room temperature. Its crystalline form makes it stable for handling under these conditions.

Melting point (Celsius)
183.00
Melting point (Kelvin)
456.00
Boiling point (Celsius)
753.90
Boiling point (Kelvin)
1 027.00
General information
Molecular weight
326.40g/mol
Molar mass
326.3950g/mol
Density
1.2538g/cm3
Appearence

Endiandric acid C appears as a white to off-white crystalline solid. Under different lighting or shading conditions, this can give off subtle variations, but it remains quite uniform in its crystalline presentation.

Comment on solubility

Solubility of (4S)-15,17-dihydroxy-4-methyl-3-oxabicyclo[12.4.0]octadeca-1(14),12,15,17-tetraene-2,8-dione

The solubility of (4S)-15,17-dihydroxy-4-methyl-3-oxabicyclo[12.4.0]octadeca-1(14),12,15,17-tetraene-2,8-dione presents intriguing characteristics that are essential for understanding its chemical behavior and potential applications. Here are some key points to consider regarding its solubility:

  • Polar vs. Nonpolar Solubility: Compounds that contain hydroxyl groups, such as this one, often exhibit increased solubility in polar solvents due to their ability to form hydrogen bonds.
  • Temperature Dependence: The solubility may vary significantly with temperature; generally, organic compounds can dissolve better in warmer conditions.
  • pH Influence: The presence of acidic or basic environments can affect the solubility of this compound, particularly through protonation and deprotonation of functional groups.
  • Solvent Compatibility: It is crucial to explore the compatibility of this compound with various solvents, as its complex structure might interact differently with solvents such as ethanol, acetone, or water.

In conclusion, the solubility of (4S)-15,17-dihydroxy-4-methyl-3-oxabicyclo[12.4.0]octadeca-1(14),12,15,17-tetraene-2,8-dione is influenced by several factors, including temperature, solvent characteristics, and the structural attributes that can facilitate solvation. Understanding these aspects allows chemists to predict and manipulate the behavior of this fascinating compound in various applications.

Interesting facts

Interesting Facts about the Compound (4S)-15,17-dihydroxy-4-methyl-3-oxabicyclo[12.4.0]octadeca-1(14),12,15,17-tetraene-2,8-dione

This highly complex compound belongs to a fascinating class of natural products known as terpenoids. These compounds are known for their unique structures and diverse biological activities. Here are some intriguing points about this compound:

  • Biological Significance: Terpenoids often play critical roles in plant defense and can possess various pharmacological properties. Some studies suggest that compounds like this one may exhibit anti-inflammatory and anti-cancer properties.
  • Stereochemistry: The detailed stereochemistry of this compound, including the (4S) chiral center, highlights the importance of spatial arrangement in chemical reactivity and biological function.
  • Complex Structure: The bicyclic structure demonstrates the compound's intricate arrangement of carbon atoms. Such complexity can lead to unique interactions with biological macromolecules.
  • Natural Sources: Similar compounds are often derived from plants and fungi, showcasing nature's remarkable ability to synthesize complex molecules with specific functional properties.
  • Potential Drug Development: The distinct functional groups in this compound, such as the hydroxyl (-OH) groups, often contribute to the interaction with biological targets, making them pivotal for medicinal chemistry.

As a result, studying compounds like (4S)-15,17-dihydroxy-4-methyl-3-oxabicyclo[12.4.0]octadeca-1(14),12,15,17-tetraene-2,8-dione not only enhances our understanding of natural product chemistry but also holds promise for future therapeutic developments. As emphasized by the acclaimed chemist Robert H. Grubbs, "Discovering novel reactions and unique compounds is the cornerstone of advancing chemical science."