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2,6-Dimethylocta-1,3,5-triene

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Identification
Molecular formula
C10H18
CAS number
762-69-0
IUPAC name
2,6-dimethylocta-1,3,5-triene
State
State

At room temperature, 2,6-Dimethylocta-1,3,5-triene exists as a liquid.

Melting point (Celsius)
-97.00
Melting point (Kelvin)
176.15
Boiling point (Celsius)
163.00
Boiling point (Kelvin)
436.15
General information
Molecular weight
122.21g/mol
Molar mass
122.2080g/mol
Density
0.7795g/cm3
Appearence

2,6-Dimethylocta-1,3,5-triene is a colorless liquid that is often clear to slightly pale yellow in color.

Comment on solubility

Solubility of 2,6-Dimethylocta-1,3,5-triene

The solubility of 2,6-dimethylocta-1,3,5-triene, a hydrocarbon compound, is primarily influenced by its non-polar characteristics. This compound belongs to the category of aliphatic hydrocarbons, which usually exhibit limited solubility in polar solvents such as water.


Key Points about Its Solubility:

  • Non-Polar Nature: As a hydrocarbon, 2,6-dimethylocta-1,3,5-triene is predominantly non-polar, leading to low solubility in polar solvents.
  • Solubility in Non-Polar Solvents: It is expected to be soluble in non-polar solvents, such as hexane and benzene, due to the principle of "like dissolves like."
  • Temperature Dependency: The solubility may increase with temperature, a common phenomenon observed with many organic compounds.

In summary, while 2,6-dimethylocta-1,3,5-triene demonstrates very limited solubility in polar media, it is well dissolved in non-polar solvents, highlighting the importance of solvent choice in chemical applications involving this compound.

Interesting facts

Interesting Facts About 2,6-Dimethylocta-1,3,5-triene

2,6-Dimethylocta-1,3,5-triene is a fascinating compound that belongs to the class of hydrocarbon compounds known as polyenes. These compounds are characterized by their alternating single and double bonds, which contribute to significant properties:

  • Natural Occurrence: This compound can be found in various natural sources, particularly in certain types of plant oils. It's interesting to note how such structural complexity plays a role in flavor and fragrance.
  • Reactivity: The structure of 2,6-dimethylocta-1,3,5-triene allows it to undergo reactions typical of alkenes, such as electrophilic addition and diels-alder reactions. This can lead to the formation of numerous derivatives, making it a versatile building block in organic synthesis.
  • Biological Significance: Compounds similar in structure are often involved in biological processes, such as photoprotective mechanisms in plants, which highlight the intersection of chemistry and biology.
  • Research Interests: Studies on 2,6-dimethylocta-1,3,5-triene often focus on its potential applications in materials science and organic photovoltaics, where its unique electronic properties can be harnessed.

As a chemistry student or scientist, exploring the properties and reactions of 2,6-dimethylocta-1,3,5-triene opens many avenues for research and understanding of complex organic reactions. Its structure can serve as a gateway to discussions about isomerism and conformational analysis as well.

In conclusion, 2,6-dimethylocta-1,3,5-triene is much more than just a simple hydrocarbon; its properties and applications make it a subject worth exploring in the vast field of organic chemistry.

Synonyms
1,3,5-Octatriene, 2,6-dimethyl-, (3Z,5E)-
121951-00-6
DTXSID30275103
RefChem:217191
DTXCID50226551
2,6-dimethyloctatriene
SCHEMBL7618519
NVQRIRLJPCDULK-UHFFFAOYSA-N