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Heptadeca-1,9,16-trien-4,6-diyn-3-ol

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Identification
Molecular formula
C17H24O
CAS number
2467-03-6
IUPAC name
heptadeca-1,9,16-trien-4,6-diyn-3-ol
State
State
The compound is in a liquid state at room temperature.
Melting point (Celsius)
-20.00
Melting point (Kelvin)
253.15
Boiling point (Celsius)
145.00
Boiling point (Kelvin)
418.15
General information
Molecular weight
244.38g/mol
Molar mass
244.3940g/mol
Density
0.8922g/cm3
Appearence

The compound is typically a colorless to pale yellow liquid. It has a slight aromatic odor characteristic of acetylenic alcohols.

Comment on solubility

Solubility of Heptadeca-1,9,16-trien-4,6-diyn-3-ol (C17H24O)

Heptadeca-1,9,16-trien-4,6-diyn-3-ol, characterized by its complex structure, exhibits distinctive solubility properties that can be intriguing for chemists and researchers alike. Its solubility can be summarized as follows:

  • Solvent Polarities: The compound is somewhat soluble in polar solvents such as methanol and ethanol, primarily due to the presence of the hydroxyl (-OH) group that enhances interactions through hydrogen bonding.
  • Non-Polar Solvents: It is generally more soluble in non-polar solvents like hexane and toluene, which is attributed to its long hydrocarbon chain that increases hydrophobic interactions.
  • Temperature Effects: Increased temperature typically enhances solubility; therefore, experiments should account for temperature variations when assessing solubility limits.

In addition, it's worth noting that the solubility of this compound is influenced by various factors such as:

  • Chain Length: The extensive carbon chain contributes significantly to the hydrophobic character.
  • Molecular Interactions: The capacity for intramolecular hydrogen bonding can further complicate solubility assessments.
  • Conformational Flexibility: The presence of multiple double and triple bonds allows for conformational variation, which may impact how the molecule interacts with solvents.

For optimal dissolution, experiments may involve a range of solvents to fully understand the solubility dynamics of heptadeca-1,9,16-trien-4,6-diyn-3-ol. Understanding these solubility characteristics is crucial for applications in organic synthesis and material science.

Interesting facts

Exploring Heptadeca-1,9,16-trien-4,6-diyn-3-ol

Heptadeca-1,9,16-trien-4,6-diyn-3-ol is an intriguing organic compound that belongs to the family of polyunsaturated alcohols. This compound is characterized by a unique structure that features both triple (-C≡C-) and double bonds (-C=C-) within its carbon chain. Here are some fascinating aspects of this chemical:

  • Natural Occurrence: Heptadeca-1,9,16-trien-4,6-diyn-3-ol is not commonly found in nature, but similar polyunsaturated alcohols are often observed in various plant and animal sources. Such compounds play essential roles in biological processes, contributing to the functions of cell membranes and signaling.
  • Importance in Research: The unique functional groups in heptadeca-1,9,16-trien-4,6-diyn-3-ol make it a subject of interest in organic chemistry and materials science. Researchers study its reactivity and potential applications in synthesizing new polymers and specialized materials.
  • Potential Applications: There is ongoing research into the uses of compounds containing multiple unsaturated bonds. Heptadeca-1,9,16-trien-4,6-diyn-3-ol can be explored for applications in drug development, as its structure may interact favorably with biological systems.
  • Synthesis Challenges: The synthesis of heptadeca-1,9,16-trien-4,6-diyn-3-ol represents a valuable exercise in mastering synthetic methods. The multiple unsaturated bonds can pose synthetic challenges, making it an excellent study topic for organic chemists.

In summary, heptadeca-1,9,16-trien-4,6-diyn-3-ol serves as a captivating example of complexity in organic compounds, bridging the gap between fundamental chemistry and its practical applications in science and technology.