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Prostaglandin H2

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Identification
Molecular formula
C20H32O5
CAS number
42935-17-1
IUPAC name
6-[5-hydroxy-4-(3-hydroxyoct-1-enyl)-3,3a,4,5,6,6a-hexahydrocyclopenta[b]furan-2-ylidene]hexanoic acid
State
State

At room temperature, Prostaglandin H2 is in a liquid state.

Melting point (Celsius)
-73.00
Melting point (Kelvin)
200.15
Boiling point (Celsius)
300.00
Boiling point (Kelvin)
573.15
General information
Molecular weight
354.47g/mol
Molar mass
354.4650g/mol
Density
1.0000g/cm3
Appearence

Prostaglandin H2 typically appears as a colorless to pale yellow viscous liquid. As with many other amniotic substances, it is sensitive to degradation and requires careful handling to maintain stability.

Comment on solubility

Solubility of 6-[5-hydroxy-4-(3-hydroxyoct-1-enyl)-3,3a,4,5,6,6a-hexahydrocyclopenta[b]furan-2-ylidene]hexanoic acid

The solubility of the compound with the formula C20H32O5 can be quite intriguing due to its complex structure and functional groups. Understanding its solubility involves considering several factors:

  • Polarity: The presence of multiple hydroxyl (–OH) groups suggests that the compound may exhibit higher polarity, which can enhance its solubility in polar solvents such as water.
  • Hydrophobic Regions: The long hydrocarbon chain (3-hydroxyoct-1-enyl) may lend some hydrophobic characteristics, indicating that the compound could also dissolve in non-polar organic solvents.
  • pH Sensitivity: As a carboxylic acid, the solubility may be influenced by the pH of the solution, potentially increasing in more alkaline conditions where the acid can ionize.

Consequently, the solubility profile of this compound could be summarized as:

  1. Soluble in polar solvents due to its hydroxyl groups.
  2. Moderately soluble in non-polar solvents due to its hydrophobic chains.
  3. Variable solubility based on the pH of the surrounding environment, with increased solubility in alkaline conditions.

In conclusion, the solubility of this compound is a product of its intricate balance between hydrophilic and hydrophobic components, making it a fascinating subject of study in the realm of chemical behavior.

Interesting facts

Exploring 6-[5-hydroxy-4-(3-hydroxyoct-1-enyl)-3,3a,4,5,6,6a-hexahydrocyclopenta[b]furan-2-ylidene]hexanoic Acid

This fascinating compound represents a remarkable intersection of organic chemistry and potential medicinal applications. Known for its complex structure, 6-[5-hydroxy-4-(3-hydroxyoct-1-enyl)-3,3a,4,5,6,6a-hexahydrocyclopenta[b]furan-2-ylidene]hexanoic acid is a naturally occurring molecule that captures the interest of researchers for several reasons:

  • Structural Complexity: The intricate formation and connection of multiple functional groups make it a prime subject for studying molecular interactions and reactivity.
  • Potential Pharmacological Properties: Early investigations suggest that derivatives of this compound may exhibit biological activity, paving the way for future drug development aimed at combating chronic diseases.
  • Source of Inspiration: As a naturally occurring compound, it serves as an inspiration for synthetic chemists who aim to replicate its structure and harness its properties.
  • Environmental Relevance: Compounds like this can be understood in the context of ecological studies, especially regarding their roles in plant metabolism and human health.

Interestingly, the hexahydrocyclopenta[b]furan moiety within its structure is particularly noteworthy. Furan derivatives have been extensively studied in medicinal chemistry because they can interact with a variety of biological targets. This broad applicability denotes why studying compounds like 6-[5-hydroxy-4-(3-hydroxyoct-1-enyl)-3,3a,4,5,6,6a-hexahydrocyclopenta[b]furan-2-ylidene]hexanoic acid is essential in the ongoing quest for new therapeutic agents.

In conclusion, the exploration of this compound not only enhances our understanding of organic chemistry but also opens up new avenues in pharmaceuticals and biochemistry.