1-ethylallylbenzene

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Identification

Molecular formula
C11H14
CAS Number
1014-92-2
IUPAC Name
1-ethylallylbenzene
Molecular Weight
146.22g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
0.8620g/cm3
Appearance
is typical of many volatile organic compounds with a benzene ring, displaying a consistency akin to other light hydrocarbons.
Synonyms
3-Phenyl-1-pentene
Interesting facts

Interesting Facts about 1-Ethylallylbenzene

1-Ethylallylbenzene is a unique aromatic compound that holds significance in both natural and synthetic realms of chemistry. Here are some captivating insights about this compound:

  • Structure and Characteristics: This compound is notable for its combination of an ethyl and an allyl group attached to a benzene ring, which makes it a type of alkenyl aromatic hydrocarbon. Its structure is responsible for reactivity and diverse chemical behavior.
  • Natural Occurrences: 1-Ethylallylbenzene is not just a lab curiosity; it can be found in nature. It has been identified in various essential oils, contributing to the characteristic fragrances of plants.
  • Chemical Reactions: The presence of both ethyl and allyl substituents allows 1-ethylallylbenzene to participate in a range of chemical reactions, including electrophilic aromatic substitution and polymerization. This versatility makes it a valuable compound for developing new materials.
  • Applications in Industry: Due to its reactive nature, this compound can be utilized in the synthesis of various organic compounds. It plays a role in the production of perfumes, flavors, and in the manufacturing of specialty chemicals.
  • Studying Mechanisms: The reactions of 1-ethylallylbenzene serve as excellent case studies for understanding fundamental organic chemistry principles, including reaction mechanisms and steric effects, making it popular among chemistry students.

In conclusion, 1-ethylallylbenzene is more than just an aromatic compound; it embodies a blend of natural chemistry and synthetic potential, making it an intriguing subject for both researchers and students alike.

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