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Farnesene epoxide

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Identification
Molecular formula
C27H46O
CAS number
39185-83-2
IUPAC name
2,2-dimethyl-3-(3,7,12,16,20-pentamethylhenicosa-3,7,11,15,19-pentaenyl)oxirane
State
State
At room temperature, Farnesene epoxide is a liquid.
Melting point (Celsius)
-39.50
Melting point (Kelvin)
233.65
Boiling point (Celsius)
297.50
Boiling point (Kelvin)
570.65
General information
Molecular weight
366.65g/mol
Molar mass
366.6450g/mol
Density
0.8867g/cm3
Appearence

Farnesene epoxide is typically found as a colorless, viscous liquid.

Comment on solubility

Solubility of 2,2-dimethyl-3-(3,7,12,16,20-pentamethylhenicosa-3,7,11,15,19-pentaenyl)oxirane

The solubility of 2,2-dimethyl-3-(3,7,12,16,20-pentamethylhenicosa-3,7,11,15,19-pentaenyl)oxirane, with the chemical formula C27H46O, is an intriguing subject due to its complex structure. Here are the key points to note about its solubility:

  • Polarity: The presence of the oxirane (epoxide) functional group suggests that the molecule may exhibit varying degrees of polarity.
  • Hydrophobic Character: Given the extensive hydrocarbon chain in the structure (including five methyl groups integral to the main pentamethylhenicosa chain), the compound likely displays hydrophobic characteristics.
  • Solvent Compatibility: Due to its hydrophobic nature, the compound is anticipated to be more soluble in non-polar or weakly polar solvents such as:
    • Hexane
    • Chloroform
    • Diethyl ether
  • Limited Water Solubility: As a result of its large hydrocarbon content, the solubility in water is expected to be quite low, which is common for similar organic compounds.

In summary, one can assert that the solubility of this compound is dictated by its structural features—characterized by a striking balance between its polar oxirane group and its extensive hydrophobic carbon framework. Understanding these aspects is crucial for applications and further research involving this compound.

Interesting facts

Interesting Facts About 2,2-Dimethyl-3-(3,7,12,16,20-pentamethylhenicosa-3,7,11,15,19-pentaenyl)oxirane

This fascinating compound, known for its intricate structure and unique properties, is a member of the oxirane family, which is also known as epoxides. Here are some noteworthy aspects of this compound:

  • Complex Structure: The name itself suggests the compound boasts a complex configuration with multiple methyl groups, which significantly influence its reactivity and stability.
  • Biological Relevance: Compounds that contain oxirane rings are of considerable interest in the field of biochemistry. These structures often participate in important metabolic processes and can function as key intermediates in synthetic organic chemistry.
  • Potential Applications: Researchers explore the applications of this compound in domains such as pharmaceuticals and material science. Given its structural features, it could serve as a precursor in synthesizing various biologically active molecules.
  • Sustainability Angle: The presence of multiple methyl groups suggests the potential for utilizing this compound in green chemistry initiatives aimed at developing sustainable synthesis routes.
  • Structural Versatility: The unique arrangement of double bonds and the oxirane functionality allows for interesting reactions such as ring-opening mechanisms, which can lead to a variety of derivatives with diverse chemical properties.

As we delve deeper into the study of this compound, it becomes evident that it is more than just a chemical; it is a gateway to understanding more complex interactions within organic chemistry and its applications in real-world scenarios. As one expert notes, “The beauty of organic chemistry lies in the creativity of its structures and the unique reactions they undergo.”

Synonyms
2,2-dimethyl-3-(3,7,12,16,20-pentamethylhenicosa-3,7,11,15,19-pentaenyl)oxirane
DTXSID70864171
2,2-dimethyl-3-(3,7,12,16,20-pentamethylhenicosa-3,7,11,15,19-pentaen-1-yl)oxirane
NS00124863