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3-cyclooctylpropan-1-ol

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Identification
Molecular formula
C11H22O
CAS number
69805-69-6
IUPAC name
3-cyclooctylpropan-1-ol
State
State

At room temperature, 3-Cyclooctylpropan-1-ol is usually found as a liquid. Its physical properties such as viscosity and lack of color make it amenable to various chemical applications.

Melting point (Celsius)
29.00
Melting point (Kelvin)
302.15
Boiling point (Celsius)
270.30
Boiling point (Kelvin)
543.45
General information
Molecular weight
156.30g/mol
Molar mass
156.2560g/mol
Density
0.9278g/cm3
Appearence

3-Cyclooctylpropan-1-ol appears as a clear to slightly pale liquid. The liquid is less viscous and typically has a mild, sweet odor. Being an alcohol, it reacts with certain reactive species but is generally stable under standard conditions.

Comment on solubility

Solubility of 3-cyclooctylpropan-1-ol

3-cyclooctylpropan-1-ol, possessing the structural formula that includes a cyclooctyl group attached to a propanol backbone, exhibits unique solubility characteristics.

Main points regarding its solubility:

  • Polarity: The hydroxyl (-OH) group present in 3-cyclooctylpropan-1-ol imparts some degree of polarity, significantly influencing its solubility in various solvents.
  • Solvent Compatibility: This compound tends to be soluble in polar solvents like water to a certain extent, but it is likely to show higher solubility in nonpolar organic solvents due to the larger hydrophobic cyclooctyl group.
  • Hydrogen Bonding: The presence of the hydroxyl group allows 3-cyclooctylpropan-1-ol to participate in hydrogen bonding, enhancing its solubility in polar environments.
  • Temperature Influence: Solubility may also vary with temperature; as temperature increases, solubility in some solvents may improve.

In conclusion, while 3-cyclooctylpropan-1-ol can be expected to be soluble in both polar and nonpolar solvents, its practical solubility levels will ultimately depend on the specific conditions and surrounding solvent characteristics.

Interesting facts

Interesting Facts About 3-Cyclooctylpropan-1-ol

3-Cyclooctylpropan-1-ol is a fascinating organic compound with a unique structure that offers numerous possibilities for scientific exploration. Here are some intriguing aspects to consider:

  • Structural Complexity: This compound features a cyclooctane ring, which contributes to its distinct molecular geometry. The incorporation of a saturated alcohol chain makes it an excellent candidate for studying conformational dynamics in organic molecules.
  • Applications: 3-Cyclooctylpropan-1-ol may have potential applications in pharmaceuticals and materials science. The presence of the cyclooctane ring can enhance the conformational flexibility of the molecule, leading to unique interactions with biological systems or in polymer formulations.
  • Research Potential: Investigating the reactivity of the alcohol functional group could lead to new synthetic pathways or modifications in related compounds, making it a valuable subject for organic synthesis.
  • Hydrophobic Character: Due to its hydrophobic nature, this compound can serve as a model for studying lipid interactions and membrane permeability, which are vital areas in biochemistry and pharmacology.
  • Synthesis: The synthesis of 3-cyclooctylpropan-1-ol may involve innovative organic reactions, showcasing the creativity of chemists in designing complex molecules. Mechanistic studies on its formation can reveal new insights into reaction pathways.
  • Literature Insight: There may be limited direct studies published specifically on this compound, but understanding its related derivatives could provide significant information on behavior and characteristics that are transferable to similar chemical structures.

In summary, 3-Cyclooctylpropan-1-ol is not just an isolated chemical entity; it is a portal into the realms of organic synthesis, pharmaceutical research, and materials innovation. The exploration of its properties and potential applications can yield exciting scientific advancements.

Synonyms
CYCLOOCTANEPROPANOL
16782-30-2
DTXSID80168379
DTXCID1090870
SCHEMBL2533487
SCHEMBL2533491
AKOS006313183