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2,5-diallyloxynorbornane

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Identification
Molecular formula
C15H24O2
CAS number
3039-72-3
IUPAC name
2,5-diallyloxynorbornane
State
State
At room temperature, this compound is in a liquid state, providing ease of use in various chemical synthesis processes.
Melting point (Celsius)
-23.00
Melting point (Kelvin)
250.15
Boiling point (Celsius)
321.00
Boiling point (Kelvin)
594.15
General information
Molecular weight
221.35g/mol
Molar mass
221.3080g/mol
Density
1.0265g/cm3
Appearence

2,5-Diallyloxynorbornane typically appears as a colorless liquid and is characterized by its lack of color and fluid nature at room temperature.

Comment on solubility

Solubility of 2,5-diallyloxynorbornane

2,5-Diallyloxynorbornane, a compound with the formula C13H18O2, exhibits interesting solubility properties that reveal a lot about its molecular structure and functionality.

This compound is primarily considered to be:

  • Moderately soluble in organic solvents: 2,5-diallyloxynorbornane shows good solubility in non-polar solvents such as hexane, benzene, and toluene. The presence of its diallyloxy functional groups contributes to this solubility.
  • Poorly soluble in water: Due to its relatively large hydrophobic (water-repelling) hydrocarbon backbone, it tends to resist dissolving in polar solvents like water. This is typical for many organic compounds with significant hydrophobic characteristics.

In summary, while 2,5-diallyloxynorbornane is soluble in various organic solvents, its limited affinity for water underscores the importance of functional groups in determining solubility. Understanding such solubility patterns is crucial for applications in organic synthesis and material science.

Interesting facts

Interesting Facts about 2,5-Diallyloxynorbornane

2,5-Diallyloxynorbornane is a fascinating compound that exhibits a unique structure and intriguing properties. Here are some key aspects that make this compound particularly interesting:

  • Structural Complexity: This compound features a norbornane skeleton, which is known for its bicyclic structure. The presence of dual allyl ether groups at the 2 and 5 positions introduces significant steric and electronic effects, making its reactivity quite distinct compared to simpler structures.
  • Synthetic Potential: Due to its unique structure, 2,5-diallyloxynorbornane serves as an important building block in organic synthesis. Its reactivity can be harnessed for developing novel materials, including polymers and pharmaceuticals.
  • Catalytic Applications: This compound has been explored in various catalytic reactions, enabling transformations that are vital in fine chemical synthesis. Its ability to participate in Diels-Alder reactions adds to its versatility, making it valuable in creating complex organic frameworks.
  • Research Interest: Scientists are keen on investigating the properties and potential applications of 2,5-diallyloxynorbornane in fields such as material science and medicinal chemistry, which highlights its importance in ongoing research.

In summary, 2,5-diallyloxynorbornane stands out due to its structural integrity, synthetic versatility, and potential applications in various scientific fields, paving the way for innovative developments in chemistry.

Synonyms
Bicyclo(2.2.1)hept-2,5-ylene, bisallyl ether
22590-50-7
BICYCLO(2.2.1)HEPTAN-2,5-DIOL, DIALLYL ETHER
RefChem:329180
SCHEMBL2575333
DTXSID80945243
2,5-Bis[(prop-2-en-1-yl)oxy]bicyclo[2.2.1]heptane