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Identification
Molecular formula
C23H38O3
CAS number
NA
IUPAC name
3-ethyl-4-(8-hydroxy-1,3,5,7,9-pentamethyl-6-oxo-undec-3-enyl)oxetan-2-one
State
State

At room temperature, this compound is a liquid.

Melting point (Celsius)
-60.00
Melting point (Kelvin)
213.15
Boiling point (Celsius)
480.00
Boiling point (Kelvin)
753.15
General information
Molecular weight
344.50g/mol
Molar mass
344.5000g/mol
Density
0.9630g/cm3
Appearence

The compound appears as a colorless to pale yellow liquid.

Comment on solubility

Solubility of 3-ethyl-4-(8-hydroxy-1,3,5,7,9-pentamethyl-6-oxo-undec-3-enyl)oxetan-2-one

The solubility of 3-ethyl-4-(8-hydroxy-1,3,5,7,9-pentamethyl-6-oxo-undec-3-enyl)oxetan-2-one, with the chemical formula C23H38O3, can be influenced by several factors. Due to its complex molecular structure, the solubility characteristics may exhibit the following behaviors:

  • Polar vs. Non-Polar Solvents: This compound may show higher solubility in non-polar solvents due to its extended hydrocarbon chains, which can enhance interactions with non-polar molecules.
  • Hydroxyl Group Impact: The presence of hydroxyl groups (-OH) in the structure can lead to improved solubility in polar solvents, like alcohols or ethers, due to hydrogen bonding capabilities.
  • Molecular Weight Consideration: With a relatively high molecular weight, the overall solubility might be limited, especially in water, as larger organic molecules often exhibit lower solubility.
  • Temperature Influence: Higher temperatures generally increase solubility. As the temperature rises, the kinetic energy of molecules increases, which may help in overcoming solubility barriers.

In summary, the solubility of 3-ethyl-4-(8-hydroxy-1,3,5,7,9-pentamethyl-6-oxo-undec-3-enyl)oxetan-2-one is likely to be moderate to high in organic solvents and can vary significantly in different polar and non-polar environments. Evaluating specific solubility conditions is essential for practical applications.

Interesting facts

Interesting Facts about 3-Ethyl-4-(8-hydroxy-1,3,5,7,9-pentamethyl-6-oxo-undec-3-enyl)oxetan-2-one

This compound, known for its intriguing structure and potential applications, falls within the category of complex organic compounds that exhibit remarkable chemical properties.

Structural Insights

  • Functional Groups: The compound features an oxetan-2-one ring, which incorporates a ketone and a hydroxyl group, supporting a range of reactivity.
  • Aliphatic Hydrocarbon Chain: The presence of a lengthy hydrocarbon chain contributes to the compound's unique properties and facilitates various interactions.
  • Conjugated System: The enone functionality allows for significant electron delocalization, potentially influencing the compound's reactivity towards electrophiles.

Potential Applications

Due to its intricate structure, this compound may possess various applications, including:

  • Pharmaceutical Development: Compounds with similar structures have been studied for their biological activity, making this one a candidate for medicinal chemistry.
  • Material Science: Its unique properties can be harnessed for creating advanced materials with tailored characteristics.

Research and Exploration

Studying 3-ethyl-4-(8-hydroxy-1,3,5,7,9-pentamethyl-6-oxo-undec-3-enyl)oxetan-2-one opens doors to numerous scientific inquiries:

  • Synthesis Techniques: The synthesis of such complex molecules provides insights into advanced synthetic methods as well as creative problem-solving skills in organic chemistry.
  • Reactivity Patterns: Understanding how this compound interacts with different reagents can advance knowledge in reaction mechanisms.

In summary, 3-ethyl-4-(8-hydroxy-1,3,5,7,9-pentamethyl-6-oxo-undec-3-enyl)oxetan-2-one is an exceptional compound that exemplifies the richness of organic chemistry, offering pathways for discovery and innovation in various scientific fields.

Synonyms
EBELACTONE B
76808-15-6
3-ethyl-4-(9-hydroxy-4,6,8,10-tetramethyl-7-oxododec-4-en-2-yl)oxetan-2-one
SCHEMBL5964653
DB-056132