Cinnamylamine

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Identification

Molecular formula
C9H11N
CAS Number
122-57-6
IUPAC Name
3-phenylprop-2-en-1-amine
Molecular Weight
133.20g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
0.9760g/cm3
Synonyms
3-phenylprop-2-en-1-amine
Interesting facts

Interesting Facts About 3-Phenylprop-2-en-1-amine

3-Phenylprop-2-en-1-amine, more commonly known as cinnamylamine, is an intriguing compound that falls into the class of aliphatic amines. Here are some captivating aspects of this compound:

  • Structural Characteristics: The compound features a unique structure characterized by a phenyl group attached to an alkene chain, which allows for specific reactivity patterns in various chemical processes.
  • Biological Importance: Cinnamylamine has been studied for its potential roles in biological systems, particularly in relation to its derivatives, which can exhibit anti-inflammatory and antioxidant activities. This makes it an area of interest in medicinal chemistry.
  • Versatile Reactivity: Due to the presence of both amine and alkene functional groups, 3-phenylprop-2-en-1-amine can participate in a variety of reactions, including electrophilic addition and nucleophilic substitution, making it highly valuable in synthetic organic chemistry.
  • Applications in Material Science: This compound can also be a precursor for polymer synthesis and other materials, showcasing the intersection of organic chemistry with material science.
  • Historical Context: Cinnamylamine gets its name from cinnamon, derived from the word “cinnamomum,” which relates to the aromatic properties its structural analogs can exhibit, reflecting the historical allure of natural compounds in chemistry.

In summary, the study of 3-phenylprop-2-en-1-amine is not just a pursuit of understanding a single compound, but rather a journey through its structural diversity, biological significance, and synthetic versatility, making it a noteworthy subject of interest for both chemists and biologists alike.

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