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Cyclododeca-1,4,8-triene

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Identification
Molecular formula
C12H18
CAS number
4904-61-4
IUPAC name
cyclododeca-1,4,8-triene
State
State

Cyclododeca-1,4,8-triene is typically a liquid at room temperature.

Melting point (Celsius)
-10.50
Melting point (Kelvin)
262.65
Boiling point (Celsius)
210.50
Boiling point (Kelvin)
483.65
General information
Molecular weight
160.26g/mol
Molar mass
160.2610g/mol
Density
0.8927g/cm3
Appearence

Cyclododeca-1,4,8-triene is a colorless liquid. It may appear clear and slightly viscous in its pure form.

Comment on solubility

Solubility of Cyclododeca-1,4,8-triene

Cyclododeca-1,4,8-triene, a cyclic hydrocarbon, exhibits interesting solubility characteristics that are worth noting. Their behavior in solvents can be influenced by several factors:

  • Solvent Type: Cyclododeca-1,4,8-triene tends to be soluble in nonpolar solvents such as hexane or toluene, due to its nonpolar nature and hydrophobic character.
  • Temperature Effects: Like many hydrocarbons, its solubility can increase with temperature, facilitating better interaction with the solvent molecules.
  • Structural Considerations: The cyclic structure of this compound contributes to its unique solubility profile, as the rigidity of the ring can affect how it interacts with various solvents.

It is generally insoluble in polar solvents, such as water, due to the significant difference in polarity between the compound and the solvent. This behavior is characteristic of many hydrocarbons, which do not form favorable interactions with polar molecules.

In summary, the solubility of cyclododeca-1,4,8-triene is influenced by the choice of solvent and temperature, showcasing typical trends observed in nonpolar organic compounds. As a quote often used in chemistry states, “Like dissolves like,” highlighting the importance of molecular compatibility in solubility.

Interesting facts

Interesting Facts about Cyclododeca-1,4,8-triene

Cyclododeca-1,4,8-triene is a fascinating compound that belongs to the class of cyclic hydrocarbons. Here are some compelling aspects of this unique compound:

  • Cyclic Structure: Cyclododeca-1,4,8-triene features a unique twelve-membered carbon ring, which sets it apart from more common cyclic hydrocarbons. Its structure provides a variety of potential applications in organic synthesis.
  • Conjugation: The alternating double bonds in its structure contribute to a degree of conjugation, which can enhance its stability and reactivity in chemical reactions. Conjugated systems often exhibit interesting electronic properties and can play crucial roles in materials science.
  • Chemical Reactivity: The presence of multiple double bonds opens the door to various chemical reactions, such as electrophilic addition and polymerization. This makes cyclododeca-1,4,8-triene an intriguing subject for research in organic chemistry.
  • Potential Applications: Due to its unique structure and reactivity, cyclododeca-1,4,8-triene might find uses in crafting innovative materials, including high-performance polymers and organic electronic devices.
  • Environmental Considerations: As a hydrocarbon, studying compounds like cyclododeca-1,4,8-triene helps chemists understand the impact of such substances on the environment and develop sustainable chemistry practices.

The study of cyclododeca-1,4,8-triene not only enriches our understanding of hydrocarbon chemistry, but it also paves the way for exciting advancements in materials science and organic synthesis. As stated by renowned chemist Robert H. Grubbs, "The chemistry is often as surprising as it is beautiful." This holds true for compounds like cyclododeca-1,4,8-triene, which continues to captivate the interest of scientists around the world.

Synonyms
1,4,8-Cyclododecatriene
SCHEMBL887151
SCHEMBL1112544
SCHEMBL1112549
SCHEMBL1112562
SCHEMBL1112698
SCHEMBL1112841
SCHEMBL1112882
SCHEMBL1112925
SCHEMBL1113010
SCHEMBL1113359
SCHEMBL1113445
SCHEMBL1541684
SCHEMBL1541817
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