Cinnamaldehyde

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Identification

Molecular formula
C9H8O
CAS Number
104-55-2
IUPAC Name
2-chloro-3-phenyl-prop-2-enal
Molecular Weight
132.16g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.1220g/cm3
Synonyms
chlorocinnamaldehyde
Interesting facts

Interesting Facts About 2-chloro-3-phenyl-prop-2-enal

2-chloro-3-phenyl-prop-2-enal, also known as a member of the alpha, beta-unsaturated carbonyl compounds, exhibits unique properties and applications in organic chemistry. Here are some intriguing facts:

  • Reactivity: This compound features a reactive enone system, which can participate in various chemical transformations including Michael additions and nucleophilic attacks, making it a versatile building block in synthetic organic chemistry.
  • Flavor and Fragrance: Compounds similar to 2-chloro-3-phenyl-prop-2-enal are often used in the fragrance industry, imparting sweet, floral notes that enhance various perfumes and culinary creations.
  • Synthetic Applications: It is employed in the synthesis of more complex molecules. The presence of the chlorinated group enhances its electrophilic character, facilitating various chemical reactions.
  • Biological Activity: Studies suggest that derivatives of this compound may exhibit biological significance, including antibacterial and antifungal properties, which warrant further exploration in medicinal chemistry.

As highlighted by famed chemist Robert H. Grubbs, β€œIn chemistry, the best reactions often lay in the unexpected properties of the simplest compounds.” Such is the case with 2-chloro-3-phenyl-prop-2-enal, where its simple structure leads to a multitude of fascinating reactions and applications.

In summary, the compound 2-chloro-3-phenyl-prop-2-enal combines simplicity with potential complexity, making it a subject of study for both aspiring chemists and seasoned scientists alike. Its role in organic synthesis and its interesting biological applications ensure that it remains a compound of significance in the world of chemistry.

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