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2-Benzylideneheptanal

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Identification
Molecular formula
C14H16O
CAS number
122-57-6
IUPAC name
2-benzylideneheptanal
State
State

This compound is typically found in a liquid state at room temperature, which is common for many compounds used in fragrance applications. Under standard conditions, it exhibits fluidity and can be easily incorporated into formulations for various consumer products.

Melting point (Celsius)
49.00
Melting point (Kelvin)
322.15
Boiling point (Celsius)
309.50
Boiling point (Kelvin)
582.65
General information
Molecular weight
216.29g/mol
Molar mass
216.3160g/mol
Density
1.0177g/cm3
Appearence

2-Benzylideneheptanal appears as a pale yellow to yellow liquid. It has a distinctive aromatic odor that is sometimes described as floral or sweet. This compound is often used in fragrance applications due to its pleasant scent profile.

Comment on solubility

Solubility of 2-benzylideneheptanal

2-benzylideneheptanal, with its unique structure, exhibits interesting solubility characteristics. Here are some key points to consider:

  • Solvent Polarity: The solubility of 2-benzylideneheptanal is significantly influenced by solvent polarity. It is more soluble in non-polar solvents due to its hydrophobic hydrocarbon chains.
  • Common Solvents: It tends to dissolve well in solvents such as:
    • Hexane
    • Toluene
    • Chloroform
  • Water Solubility: This compound shows very low solubility in water, which is typical for organic compounds with large hydrophobic components.
  • Temperature Factor: Temperature can also play a role; higher temperatures generally increase solubility in organic solvents.

In conclusion, when working with 2-benzylideneheptanal, it is important to choose the appropriate solvent based on its non-polar characteristics. Remember, the interactions with solvents will dictate the behavior of this compound in various chemical processes.

Interesting facts

Interesting Facts about 2-benzylideneheptanal

2-benzylideneheptanal is a fascinating compound that has captured the attention of chemists and researchers alike. This organic molecule serves as an example of an α,β-unsaturated aldehyde, which presents unique reactivity patterns due to the conjugated double bond system associated with the carbonyl group. Here are some key points about this intriguing compound:

  • Versatile Building Block: 2-benzylideneheptanal serves as a versatile precursor in organic synthesis, often utilized in the synthesis of more complex molecules. Its structure allows for various functional group transformations, making it valuable in the pharmaceutical and chemical industries.
  • Mechanistic Insights: The reactivity of this compound can provide insights into catalytic cycles and reaction mechanisms. Chemists can study how it participates in reactions like Michael additions and nucleophilic attacks due to the electrophilic nature of the carbonyl carbon.
  • Applications in Research: Compounds like 2-benzylideneheptanal are often used in the development of chemosensors and ligands due to their ability to bind to metal ions, thereby participating in coordination chemistry.
  • Natural Analogues: Some derivatives of 2-benzylideneheptanal are analogous to natural products, which highlights the importance of studying such compounds to understand biological processes or develop bioactive molecules.

In summary, 2-benzylideneheptanal is more than just a simple molecule; it is a gateway into the complex world of organic chemistry, offering opportunities for synthesis, mechanistic studies, and various applications in research. Its significance extends beyond the lab bench, influencing fields from medicinal chemistry to materials science.

Synonyms
alpha-Amylcinnamaldehyde
2-Benzylideneheptanal
122-40-7
Amylcinnamaldehyde
Heptanal, 2-(phenylmethylene)-
alpha-Pentylcinnamaldehyde
DTXSID8029157
Amyl cinnamic aldehyde
2-(phenylmethylidene)heptanal
FEMA No. 2061
a-amylcinnamaldehyde
alpha-Amylcinnamic aldehyde
DTXCID409157
NSC-6649
Pentyl cinnamaldehyde
alpha -amylcinnamaldehyde
alpha-amyl-cinnamaldehyde
RefChem:1076959
2-Amyl-3-phenylacrylaldehyde
2-Amyl-3-phenyl-2-propenal
SCHEMBL113320
orb1705848
SCHEMBL2534838
CHEMBL3183519
CHEBI:196097
AKOS028108415
NCI60_022351
DB-041667
A0851
NS00079153
alpha-Amylcinnamaldehyde (mixture of cis and trans)