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2-Cyclohex-3-en-1-ylacetaldehyde

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Identification
Molecular formula
C8H12O
CAS number
-
IUPAC name
2-cyclohex-3-en-1-ylacetaldehyde
State
State
At room temperature, 2-cyclohex-3-en-1-ylacetaldehyde is in a liquid state.
Melting point (Celsius)
-63.00
Melting point (Kelvin)
210.15
Boiling point (Celsius)
229.50
Boiling point (Kelvin)
502.65
General information
Molecular weight
138.21g/mol
Molar mass
138.2060g/mol
Density
0.9686g/cm3
Appearence

2-Cyclohex-3-en-1-ylacetaldehyde appears as a colorless to pale yellow liquid. It typically has a fruity or floral odor and is used in the fragrance industry.

Comment on solubility

Solubility of 2-cyclohex-3-en-1-ylacetaldehyde

2-cyclohex-3-en-1-ylacetaldehyde, with its unique structure, exhibits solubility characteristics that reflect its chemical nature. This compound is moderately soluble in a variety of organic solvents, marking it as notably suited for applications in organic synthesis and chemical reactions. Here are some key points regarding its solubility:

  • Solvent Compatibility: It is primarily soluble in non-polar to moderately polar solvents, such as hexane, methanol, and dichloromethane.
  • Temperature Influence: As with many organic compounds, its solubility can increase with temperature, making warm solvents more effective for dissolving the compound.
  • Functional Groups Role: The presence of the aldehyde functional group increases the potential for interactions with polar solvents, potentially enhancing its solubility in those mediums.

In essence, if you are considering the use of 2-cyclohex-3-en-1-ylacetaldehyde in a reaction or formulation, it is essential to select the appropriate solvent to maximize its solubility and reactivity. As a general reference, "the versatility of the solvent can significantly affect the performance of the compound in various chemical processes."

Interesting facts

Exploring 2-cyclohex-3-en-1-ylacetaldehyde

2-cyclohex-3-en-1-ylacetaldehyde is a fascinating compound that captures the attention of chemists and researchers alike. Here are some intriguing aspects of this compound:

  • Structural uniqueness: The presence of a cyclohexene ring and an aldehyde functional group gives this compound distinct characteristics, making it of particular interest in organic synthesis.
  • Reactivity: As an aldehyde, 2-cyclohex-3-en-1-ylacetaldehyde is likely to undergo various chemical reactions, such as nucleophilic addition, which can lead to the formation of more complex molecules.
  • Applications: This compound may find applications in the field of fragrances and flavors, as aldehydes are often key intermediates in the synthesis of aromatic compounds.
  • Precursor potential: Its unique structure offers the potential to act as a precursor for various natural products or pharmaceuticals, making it a compound of interest in medicinal chemistry.

As the renowned chemist Linus Pauling once said, "The best way to have a good idea is to have lots of ideas." Exploring the diverse chemical properties and applications of compounds like 2-cyclohex-3-en-1-ylacetaldehyde can lead to innovative discoveries.

In conclusion, the study of 2-cyclohex-3-en-1-ylacetaldehyde showcases the beauty and complexity of organic chemistry, inviting further exploration and research in this vibrant field.

Synonyms
24480-99-7
Acetaldehyde, 3-cyclohexen-1-yl-
RefChem:1075183
3-CYCLOHEXENE-1-ACETALDEHYDE
3-Cyclohexen-1-ylacetaldehyde
SCHEMBL4402509
3-Cyclohexen-1-ylacetaldehyde #
DTXSID90947379
UPVGDGITFOERJA-UHFFFAOYSA-N
(Cyclohex-3-en-1-yl)acetaldehyde
2-(1-cyclohex-3-enyl)-acetaldehyde
2-(CYCLOHEX-3-EN-1-YL)ACETALDEHYDE
EN300-1829687