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Ketoisophorone

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Identification
Molecular formula
C13H16O3
CAS number
1461-23-0
IUPAC name
6-acetyl-3a,5a-dimethyl-3b,4,5,6,7,8,8a,8b,9,10-decahydro-3H-indeno[5,4-e]inden-2-one
State
State

At room temperature, Ketoisophorone is in a liquid state. It is also known to have a distinct and potent odor, characteristic of ketone compounds.

Melting point (Celsius)
-8.00
Melting point (Kelvin)
265.15
Boiling point (Celsius)
239.00
Boiling point (Kelvin)
512.15
General information
Molecular weight
164.22g/mol
Molar mass
164.2200g/mol
Density
1.0301g/cm3
Appearence

Ketoisophorone is a pale yellow, oily liquid that can appear slightly viscous due to its organic structure. Its coloration can vary slightly depending on the purity and conditions.

Comment on solubility

Solubility of 6-acetyl-3a,5a-dimethyl-3b,4,5,6,7,8,8a,8b,9,10-decahydro-3H-indeno[5,4-e]inden-2-one

The solubility of 6-acetyl-3a,5a-dimethyl-3b,4,5,6,7,8,8a,8b,9,10-decahydro-3H-indeno[5,4-e]inden-2-one can be a multifaceted topic due to its complex molecular structure. In general, the solubility of such organic compounds can depend on several factors:

  • Polarity: Nonpolar compounds tend to dissolve in nonpolar solvents, while polar compounds are soluble in polar solvents. This compound is likely to exhibit limited solubility in polar solvents due to its extensive hydrophobic regions.
  • Temperature: An increase in temperature often enhances solubility for many compounds. As the kinetic energy of the molecules increases, interactions between solute and solvent may become more favorable.
  • Solvent Choice: Common solvents which might aid in dissolving this compound include organic solvents such as ethanol, acetone, or chloroform. The effectiveness of the solvent varies based on its interaction with the solute.
  • Functional Groups: The presence of specific functional groups like the acetyl group may enhance solubility in polar organic solvents, despite the overall presence of a large hydrophobic framework.

In conclusion, the solubility of this compound is likely to be limited, particularly in water, but it could find better solubility in organic solvents. Awareness of these factors can significantly improve the approach to solubility testing and practical applications in synthesis and formulation.

Interesting facts

Interesting Facts about 6-Acetyl-3a,5a-Dimethyl-3b,4,5,6,7,8,8a,8b,9,10-Decahydro-3H-Indeno[5,4-e]Inden-2-One

This intriguing compound, commonly referred to within specialized circles, is renowned for its unique structural features which make it a point of interest in organic chemistry. Here are some fascinating details:

  • Complex Structure: The compound is characterized by its complex multi-ring system, which contributes to its unique chemical and physical properties.
  • Synthesis: The synthetic pathways to produce this compound are often regarded as challenging yet rewarding, providing insight into advanced organic synthesis techniques.
  • Applications: Compounds in this class are frequently explored for their potential biological activities, including uses in pharmaceuticals and flavoring agents.
  • Isomerism: Given its intricate stereochemistry, the compound presents numerous isomeric forms, each with distinct properties and reactivity.
  • Research Interest: Postulated interactions with various biological systems have deservingly made this compound a subject of ongoing research in the fields of medicinal chemistry and material science.

One particularly exciting aspect of studying such complex molecules is understanding their behavior in various environments and the implications this has for both theoretical and practical applications. Either through its chemical transformations or potential applications, compounds like 6-Acetyl-3a,5a-dimethyl-3b,4,5,6,7,8,8a,8b,9,10-decahydro-3H-Indeno[5,4-e]Inden-2-one exemplify the dynamic nature of organic chemistry.

In summary, the exploration of this compound not only enhances our understanding of chemical diversity but also opens the door for further innovations in science and technology.

Synonyms
A-Norpregn-3(5)-ene-3,20-dione
NSC48015