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2,6-Dioxaspiro[3.3]heptane

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Identification
Molecular formula
C5H8O2
CAS number
592-09-6
IUPAC name
2,6-dioxaspiro[3.3]heptane
State
State

At room temperature, 2,6-dioxaspiro[3.3]heptane is a liquid.

Melting point (Celsius)
-60.00
Melting point (Kelvin)
213.15
Boiling point (Celsius)
98.00
Boiling point (Kelvin)
371.15
General information
Molecular weight
86.12g/mol
Molar mass
86.0900g/mol
Density
1.1202g/cm3
Appearence

2,6-Dioxaspiro[3.3]heptane is a colorless liquid at room temperature.

Comment on solubility

Solubility of 2,6-Dioxaspiro[3.3]heptane

When discussing the solubility of 2,6-dioxaspiro[3.3]heptane, it is important to consider its unique structural characteristics which influence its behavior in various solvents. This compound typically demonstrates the following solubility traits:

  • Polarity: The presence of dioxole rings contributes to the overall polarity of the molecule, enhancing solubility in polar solvents like water and alcohols.
  • Hydrophobic Interactions: The spiro structure introduces hydrophobic regions that may limit solubility in highly lipophilic solvents, making it less soluble in nonpolar solvents such as hexane or benzene.
  • Temperature Dependence: As with many organic compounds, solubility can be affected by temperature. Generally, increased temperatures lead to higher solubility levels in solvents.

In summary, the solubility of 2,6-dioxaspiro[3.3]heptane is influenced by its polarity, hydrophobic regions, and environmental conditions such as temperature. Understanding these factors is crucial for predicting its behavior in chemical processes and applications.

Interesting facts

Interesting Facts about 2,6-Dioxaspiro[3.3]heptane

2,6-Dioxaspiro[3.3]heptane is a fascinating compound that showcases the complexity and beauty of organic chemistry. Its unique structure and properties make it a topic of intrigue for both researchers and students alike. Here are some of the most interesting aspects of this compound:

  • Structural Uniqueness: The compound features a spirocyclic structure, which consists of two rings sharing a single atom. This particular arrangement can impact the compound's reactivity and stability.
  • Applications in Chemistry: 2,6-Dioxaspiro[3.3]heptane has served as a building block in organic synthesis, offering pathways to create more complex molecules, including pharmaceuticals and advanced materials.
  • Synthesis Challenges: The synthesis of this compound can be somewhat intricate, often requiring a strategic approach to assemble the rings correctly without disrupting the delicate balance of functional groups.
  • Research Interest: Due to its spiro structure, it has been studied for its potential applications in various fields, including drug discovery and material sciences.
  • Inherent Properties: Compounds like 2,6-Dioxaspiro[3.3]heptane often demonstrate interesting physical and chemical properties, making them valuable for further studies in reaction mechanisms and molecular interactions.

As you delve deeper into the world of 2,6-Dioxaspiro[3.3]heptane, remember that each research endeavor contributes to our understanding of the intricate dance of atoms and bonds that define organic compounds. It beautifully illustrates the saying: "In chemistry, the smallest things make the biggest difference."

Synonyms
2,6-dioxaspiro[3.3]heptane
174-79-8
2,6-DIOXASPIRO(3.3)HEPTANE
BRN 0103147
UNII-4046SYP4FC
4046SYP4FC
MFCD01730191
DTXSID40169741
4-19-00-00114 (Beilstein Handbook Reference)
SCHEMBL799418
DTXCID1092232
AKOS015840970
AB09876
PS-9395
SY318891
2,6-Dioxaspiro[3.3]heptane, AldrichCPR
DB-003245
Q27258280