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Prostaglandin F2α

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Identification
Molecular formula
C20H34O5
CAS number
551-11-1
IUPAC name
7-(5-oct-2-enylidene-4-oxo-cyclopent-2-en-1-yl)hept-5-enoic acid
State
State

At room temperature, Prostaglandin F2α is generally in a liquid state. It can crystallize upon cooling or under certain storage conditions, depending on its formulation and concentration.

Melting point (Celsius)
70.00
Melting point (Kelvin)
343.15
Boiling point (Celsius)
168.00
Boiling point (Kelvin)
441.15
General information
Molecular weight
354.50g/mol
Molar mass
354.4990g/mol
Density
1.1400g/cm3
Appearence

Prostaglandin F2α typically appears as a colorless to pale yellow liquid, although it can also be presented in the form of an amorphous powder when isolated. It can also exhibit some slight odor depending on the type and purity of the sample.

Comment on solubility

Solubility of 7-(5-oct-2-enylidene-4-oxo-cyclopent-2-en-1-yl)hept-5-enoic acid

The solubility of the compound 7-(5-oct-2-enylidene-4-oxo-cyclopent-2-en-1-yl)hept-5-enoic acid, with the chemical formula C20H34O5, can be quite intriguing due to its unique structural features. Several factors influence its solubility:

  • Molecular Size: With a relatively large molecular weight and complex structure, solubility in water is expected to be low.
  • Polarity: The presence of the carboxylic acid functional group (-COOH) suggests potential for hydrogen bonding, enhancing solubility in polar solvents like water.
  • Hydrophobic Interactions: The long hydrocarbon chain could contribute to hydrophobic characteristics, making it less soluble in aqueous environments.
  • Solvent Compatibility: It may exhibit higher solubility in organic solvents such as ethanol, methanol, and acetone due to its hydrophobic regions.

In summary, while amphipathic characteristics suggest some degree of solubility in polar media, the overall solubility behavior of this compound likely skews towards greater compatibility with non-polar organic solvents. As a result, understanding the interactions at play is key for practical applications.

Interesting facts

Interesting Facts about 7-(5-oct-2-enylidene-4-oxo-cyclopent-2-en-1-yl)hept-5-enoic acid

This intriguing compound falls into the category of complex organic acids, showcasing a fascinating combination of structural features. Here are some key points that highlight its uniqueness:

  • Structural Composition: The compound contains a cyclopentene ring, along with an octene side chain, leading to a unique configuration that may impart interesting reactive characteristics.
  • Synthetic Potential: Due to its intricate structure, this acid may serve as a precursor for synthesizing other organic compounds, particularly in fields like medicinal chemistry and material science.
  • Reactivity: The presence of multiple functional groups could enable diverse chemical reactions, including condensation, oxidation, and Michael additions, making it a valuable compound for chemical research.
  • Biological Activity: Structurally similar compounds are often investigated for biological activity. It's possible this acid could exhibit properties useful in pharmaceuticals, such as anti-inflammatory or antimicrobial effects.

Furthermore, the elegance of its name reflects a rich tapestry of chemical relationships, showcasing how organic compounds often tell a story through their nomenclature. The exploration of such compounds can lead to a deeper understanding of their potential applications and the fundamental principles of organic chemistry.

In summary, 7-(5-oct-2-enylidene-4-oxo-cyclopent-2-en-1-yl)hept-5-enoic acid is not just a compound; it represents an exciting intersection of chemistry and potential innovation.

Synonyms
7-(5-oct-2-enylidene-4-oxo-1-cyclopent-2-enyl)-5-heptenoic acid
908084-00-4
15d-PGJ2;15-Deoxy-Delta12,14-PGJ2
DTXSID90861102
PD015643
PD194748
NS00016930
11-oxoprosta-5,9,12,14-tetraen-1-oic acid
Q27166979