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3-ethynylhept-1-en-3-ol

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Identification
Molecular formula
C9H14O
CAS number
5327-10-4
IUPAC name
3-ethynylhept-1-en-3-ol
State
State

3-Ethynylhept-1-en-3-ol is a liquid at room temperature.

Melting point (Celsius)
-50.00
Melting point (Kelvin)
223.15
Boiling point (Celsius)
198.00
Boiling point (Kelvin)
471.15
General information
Molecular weight
124.19g/mol
Molar mass
124.1930g/mol
Density
0.8996g/cm3
Appearence

3-Ethynylhept-1-en-3-ol is typically a liquid at room temperature.

Comment on solubility

Solubility of 3-ethynylhept-1-en-3-ol

3-ethynylhept-1-en-3-ol, with the chemical formula C9H10O, exhibits interesting solubility characteristics that are vital for its application in various chemical reactions and synthesis processes. Understanding the solubility of this compound can be approached by considering the following factors:

  • Polarity: The presence of the hydroxyl (–OH) group increases the polarity of the molecule, which tends to enhance solubility in polar solvents like water.
  • Hydrocarbon Chain: The hydrophobic hydrocarbon tail of 3-ethynylhept-1-en-3-ol reduces its overall solubility in water and makes it more soluble in organic solvents such as ethanol, ether, and acetone.
  • Temperature: Solubility can often be temperature-dependent; generally, as temperature increases, solubility in organic solvents increases.

In practical terms, it is noted that while 3-ethynylhept-1-en-3-ol is less soluble in water, it can be effectively dissolved in organic media, which is a critical consideration for applications in organic synthesis. Consequently, it is essential to choose the appropriate solvent for reactions or processes that involve this compound, ensuring optimal solubility conditions for successful outcomes.

Interesting facts

Interesting Facts about 3-ethynylhept-1-en-3-ol

3-ethynylhept-1-en-3-ol is a fascinating compound that belongs to the class of organic compounds known as alcohols and alkyne derivatives. Here are some intriguing aspects that highlight the significance and versatility of this compound:

  • Structural Diversity: This compound boasts a unique structure featuring both an alcohol functional group and a triple bond, making it a key player in organic synthesis.
  • Reactivity: The presence of the triple bond (alkyne) lends itself to various chemical reactions such as hydroboration, oxidation, and hydrogenation, expanding its accessibility to diverse chemical transformations.
  • Applications in Synthesis: 3-ethynylhept-1-en-3-ol can serve as a starting material for the synthesis of more complex organic molecules. Its reactive sites allow for innovative approaches in constructing functionalized compounds.
  • Natural Product Inspiration: Compounds with similar structures can often be found in nature, leading to potential applications in pharmaceuticals and biochemistry, inspiring natural product synthesis.

When discussing this compound, scientists often emphasize its versatility in research and application. As one chemist noted, "The interplay between functional groups in 3-ethynylhept-1-en-3-ol exemplifies the creativity inherent in organic chemistry." This compound is a prime example of how molecular architecture can dictate reactivity and utility in chemical applications.

In conclusion, 3-ethynylhept-1-en-3-ol serves as an exciting hub for research, highlighting the endless possibilities within organic chemistry.

Synonyms
3-Ethynyl-1-hepten-3-ol
6929-27-7
3-ethynylhept-1-en-3-ol
BRN 1749057
1-HEPTEN-3-OL, 3-ETHYNYL-
DTXSID10989014