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2-Benzylideneoctanal

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Identification
Molecular formula
C16H20O
CAS number
122-57-6
IUPAC name
2-benzylideneoctanal
State
State

At room temperature, 2-Benzylideneoctanal is a liquid. It is relatively stable under normal conditions but should be stored in a cool, dry place to extend its shelf life and prevent any degradation. Typically, it is found in research settings or the fragrance industry.

Melting point (Celsius)
-37.00
Melting point (Kelvin)
236.15
Boiling point (Celsius)
332.30
Boiling point (Kelvin)
605.45
General information
Molecular weight
236.33g/mol
Molar mass
216.3230g/mol
Density
0.9482g/cm3
Appearence

2-Benzylideneoctanal appears as a pale yellow liquid. The compound has a characteristic aromatic odor, which can be attributed to its benzylidene group. It is typically used in fragrance formulations and can vary slightly in hue depending on its purity and storage conditions. When exposed to air and light, it may degrade or become darker.

Comment on solubility

Solubility of 2-benzylideneoctanal

Understanding the solubility of 2-benzylideneoctanal, a compound characterized by its unique structure, provides insights into its behavior in various solvents. This compound is usually non-polar due to the presence of the long hydrophobic octanal chain and the aromatic benzyl group. Consequently, we can make some noteworthy observations:

  • Solvent Interaction: 2-benzylideneoctanal is expected to display significant solubility in non-polar solvents such as hexane, benzene, and toluene.
  • Poor Water Solubility: Given its hydrophobic nature, this compound is anticipated to have markedly low solubility in polar solvents like water, forming minimal interactions with water molecules.
  • Application Insights: The solubility characteristics can influence its applications in fields like organic synthesis, where compatibility with certain solvents determines the reaction conditions.

In conclusion, the solubility of 2-benzylideneoctanal highlights the pivotal role of molecular structure in determining how a compound interacts with various environments. As with many organic substances, the balance between polar and non-polar characteristics will guide its solubility profile.

Interesting facts

Interesting Facts about 2-Benzylideneoctanal

2-Benzylideneoctanal is a fascinating organic compound that plays an intriguing role in both synthetic chemistry and natural product synthesis. Here are some remarkable aspects of this compound:

  • Structural Beauty: The molecular structure of 2-benzylideneoctanal features a unique combination of an aldehyde group and a benzylidene moiety, which contributes to its reactivity and potential applications in aldol reactions.
  • Aromatic Character: The presence of a benzylidene group allows for the compound to exhibit aromatic properties, which can significantly influence its aroma profile, making it of interest in flavor and fragrance chemistry.
  • Origin of Synthesis: This compound can be synthesized through the condensation of aromatic aldehydes with aliphatic aldehydes, showcasing the beauty of organic synthesis and the diversity of carbon-carbon bond formation.
  • Applications in Organic Chemistry: 2-Benzylideneoctanal acts as a versatile intermediate in the production of complex organic molecules, opening doors to pharmaceuticals and other valuable compounds.
  • Research Significance: Studies have shown that compounds similar to 2-benzylideneoctanal can exhibit biological activities, granting them potential as leads in drug discovery.

As a compound that bridges the realms of synthetic chemistry and potential biological applications, 2-benzylideneoctanal certainly ignites curiosity within the scientific community. Its ability to participate in a variety of reactions makes it a valuable contributor to the field of organic synthesis.

Synonyms
alpha-Hexylcinnamaldehyde
101-86-0
2-Benzylideneoctanal
2-(Phenylmethylidene)octanal
Octanal, 2-(phenylmethylene)-
2-(Phenylmethylene)octanal
.alpha.-Hexylcinnamaldehyde
hexyl cinnamaldehyde
a-hexylcinnamaldehyde
DTXSID4026684
alpha-hexyl-cinnamaidehyde
alpha-hexyl-cinnamaldehyde
alpha-n-hexyl cinnamaldehyde
SCHEMBL113171
CHEMBL3183766
AKOS028108454
NCGC00247907-01
NS00002490