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Methyl jasmonate

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Identification
Molecular formula
C13H20O3
CAS number
39924-52-2
IUPAC name
methyl 7-[3-hydroxy-2-(3-hydroxy-4,4-dimethyl-oct-1-enyl)-5-oxo-cyclopentyl]hept-2-enoate
State
State

At room temperature, methyl jasmonate is typically found as a liquid.

Melting point (Celsius)
-8.00
Melting point (Kelvin)
265.15
Boiling point (Celsius)
140.00
Boiling point (Kelvin)
413.00
General information
Molecular weight
224.30g/mol
Molar mass
224.3160g/mol
Density
0.9647g/cm3
Appearence

Methyl jasmonate is a colorless to pale yellow liquid. It has a floral fragrance, reminiscent of jasmine, from which it derives its common name.

Comment on solubility

Solubility Overview

The compound methyl 7-[3-hydroxy-2-(3-hydroxy-4,4-dimethyl-oct-1-enyl)-5-oxo-cyclopentyl]hept-2-enoate (C13H20O3) exhibits specific solubility characteristics influenced by its molecular structure. Understanding these characteristics can provide insight into its potential applications and reactivity.

Solubility Insights:

  • Polar vs. Nonpolar: Given the presence of multiple hydroxyl (–OH) groups, this compound demonstrates polar characteristics, which may enhance its solubility in polar solvents such as water and ethanol.
  • Hydrophobic Regions: The hydrocarbon sections, including its long aliphatic chains, suggest that the compound also possesses hydrophobic properties, which may lead to limited solubility in nonpolar solvents like hexane.
  • Temperature Dependence: As with many organic compounds, solubility may increase with temperature. This factor can be critically important during reactions or formulations involving this compound.
  • Concentration Effects: At higher concentrations, precipitation may occur due to saturation points in a given solvent, emphasizing the need for careful formulation considerations.

Overall, the solubility of methyl 7-[3-hydroxy-2-(3-hydroxy-4,4-dimethyl-oct-1-enyl)-5-oxo-cyclopentyl]hept-2-enoate is a balance between its polar and nonpolar aspects, making it essential to consider both the solvent characteristics and the specific environment in which this compound is employed.

Interesting facts

Interesting Facts about Methyl 7-[3-hydroxy-2-(3-hydroxy-4,4-dimethyl-oct-1-enyl)-5-oxo-cyclopentyl]hept-2-enoate

Methyl 7-[3-hydroxy-2-(3-hydroxy-4,4-dimethyl-oct-1-enyl)-5-oxo-cyclopentyl]hept-2-enoate, a complex ester, showcases fascinating attributes that reflect the intricate world of organic chemistry. This compound is notable not only for its structure but also for its potential applications in various fields. Here are some compelling points about this fascinating molecule:

  • Structural Complexity: The compound features a cyclopentyl ring and a unique substitution pattern that contributes to its chemical uniqueness. The presence of multiple hydroxyl groups and a ketone enhances its reactivity.
  • Natural Product Precursor: Similar compounds are often found in nature, suggesting that this molecule might serve as an important intermediate in the synthesis of naturally occurring products or pharmaceuticals.
  • Applications in Synthesis: The functional groups present in this compound open doors to various synthetic pathways, particularly in the field of medicinal chemistry and the development of new drugs.
  • Biological Activity: Compounds like this often exhibit significant biological activity, potentially serving roles in plant biochemistry or as frameworks for the development of new therapeutic agents.

As a scientist delving into the world of organic compounds, understanding the synthesis and applications of such complex molecules can be thrilling. Discussions around the reactivity and potential uses of compounds like methyl 7-[3-hydroxy-2-(3-hydroxy-4,4-dimethyl-oct-1-enyl)-5-oxo-cyclopentyl]hept-2-enoate can inspire future research and innovations. Embracing the intricacies of such substances is crucial for advancements in chemical science.

Synonyms
ONO 802; Preglandin; SC 37681
DTXSID50867069
BCP28562
methyl 11,15-dihydroxy-16,16-dimethyl-9-oxoprosta-2,13-dien-1-oate