Cinnamyl Cinnamate

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Identification

Molecular formula
C18H16O2
CAS Number
122-69-0
IUPAC Name
cinnamyl 3-phenylprop-2-enoate
Molecular Weight
236.30g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.0863g/cm3
Synonyms
2-Propenoic acid, 3-phenyl-, 3-phenyl-2-propenyl ester
Interesting facts

Exploring Cinnamyl 3-phenylprop-2-enoate

Cinnamyl 3-phenylprop-2-enoate, a captivating compound in the realm of organic chemistry, is noteworthy for its applications and distinct structure. Here are some intriguing facts about this compound:

  • Cultural significance: This compound serves as a key component in the synthesis of various fragrances and flavoring agents. Its sweet, spicy aroma is reminiscent of cinnamon, making it valuable in the perfume and food industries.
  • Natural occurrences: Cinnamyl derivatives are often found in nature, particularly in essential oils derived from plants like cinnamon. Their natural origins add to their appeal in products aiming for a more holistic approach.
  • Reactivity: This compound showcases a unique reactivity profile, often engaging in chemical reactions such as polymerization. These reactions play a critical role in the development of new materials and polymers.
  • Research interest: Studies have indicated the potential of cinnamyl compounds in anti-inflammatory and antimicrobial research, paving the way for innovative medicines and health supplements.
  • Biotechnological applications: Due to its structure, cinnamyl 3-phenylprop-2-enoate can be modified enzymatically, making it an exciting candidate for biocatalysis in sustainable chemical processes.

As a compound that bridges the realms of chemistry, biology, and industry, cinnamyl 3-phenylprop-2-enoate exemplifies how organic compounds can not only provide benefits in their raw forms but can also lead to breakthroughs in various fields.

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