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Decahydronaphtho[2,3-b]oxirene

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Identification
Molecular formula
C10H16O
CAS number
58202-54-5
IUPAC name
1a,2,2a,3,4,5,6,6a,7,7a-decahydronaphtho[2,3-b]oxirene
State
State

At room temperature, decahydronaphtho[2,3-b]oxirene is in a liquid state.

Melting point (Celsius)
-25.00
Melting point (Kelvin)
248.10
Boiling point (Celsius)
218.50
Boiling point (Kelvin)
491.70
General information
Molecular weight
150.24g/mol
Molar mass
150.2370g/mol
Density
0.8998g/cm3
Appearence

Decahydronaphtho[2,3-b]oxirene is typically a colorless liquid with no distinct visual features. It may have a mild odor characteristic of epoxides.

Comment on solubility

Solubility of 1a,2,2a,3,4,5,6,6a,7,7a-decahydronaphtho[2,3-b]oxirene

The solubility of 1a,2,2a,3,4,5,6,6a,7,7a-decahydronaphtho[2,3-b]oxirene is an intriguing topic due to its complex structure and hydrophobic characteristics. As a compound with multiple ring systems, it is important to consider several factors that influence its solubility:

  • Non-polar Nature: The extensive hydrophobic regions in its molecular structure contribute to low solubility in polar solvents such as water.
  • Hydrocarbon Chains: Being composed primarily of hydrocarbon moieties enhances its solubility in non-polar organic solvents like hexane or chloroform.
  • Temperature Dependency: Solubility can increase with higher temperatures, but the actual increase may vary significantly based on the solvent used.

In summary, while 1a,2,2a,3,4,5,6,6a,7,7a-decahydronaphtho[2,3-b]oxirene is likely to exhibit minimal solubility in water, it shows favorable interactions with organic solvents. As a result, practical applications may often rely on its behavior in specific non-polar environments.

Interesting facts

Exploring 1a,2,2a,3,4,5,6,6a,7,7a-Decahydronaphtho[2,3-b]oxirene

This fascinating compound, known as 1a,2,2a,3,4,5,6,6a,7,7a-decahydronaphtho[2,3-b]oxirene, is intriguing for several reasons, particularly for its unique structural features and potential applications. Here are some key highlights:

  • Cyclic Structure: The compound is characterized by a bicyclic structure which includes both naphthalene and epoxide moieties. This combination contributes to its interesting reactivity and stability.
  • Natural Product Derivative: It has been studied for its resemblance to various natural products, raising interest in its potential role in medicinal chemistry and organic synthesis.
  • Reactivity: The presence of an oxirane (epoxide) functionality introduces unique chemical reactivity. This can be exploited in various organic transformations, including ring-opening reactions which may lead to diverse functional groups.
  • Synthetic Pathways: Researchers have explored various synthetic methods to construct this compound, highlighting important advancements in synthetic organic chemistry and the methodologies for producing complex molecules.
  • Applications in Materials Science: With its intricate structure, the compound holds promise in developing new materials due to its interesting mechanical and thermal properties, which could be leveraged in polymers or coatings.

In the words of chemists, “Structure dictates function,” and the intricate architecture of 1a,2,2a,3,4,5,6,6a,7,7a-decahydronaphtho[2,3-b]oxirene certainly supports this principle. The ongoing exploration into this compound not only deepens our understanding of organic chemistry but also paves the way for innovative applications in various fields.

Synonyms
Decahydronaphtho[2,3-b]oxirene
21399-51-9
Decahydronaphtho(2,3-b)oxirene
DTXSID00943948
RefChem:336686
DTXCID601372305
1a,2,2a,3,4,5,6,6a,7,7a-decahydronaphtho[2,3-b]oxirene
SCHEMBL172869
OQOKLVGYVIWSPZ-UHFFFAOYSA-N
Decahydronaphtho[2,3-b]oxirene #
Naphth[2,3-b]oxirene, decahydro-
Naphthalene, 2,3-epoxydecahydro-, trans-(.+/-.)-