1-(2-Pentoxyphenyl)ethanone

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Identification

Molecular formula
C13H18O2
CAS Number
37643-29-7
IUPAC Name
1-(2-pentoxyphenyl)ethanone
Molecular Weight
190.25g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.0120g/cm3
Synonyms
2'-Pentyloxyacetophenone
Interesting facts

Interesting Facts about 1-(2-pentoxyphenyl)ethanone

1-(2-pentoxyphenyl)ethanone, a compound of interest in organic chemistry, showcases the intriguing interplay between structure and reactivity in chemical compounds.

Key Features

  • Functional Group Variety: This compound contains both an aromatic ring and a ketone functional group, which can influence its reactivity and properties. The aromatic nature often imparts stability and distinct electronic characteristics.
  • Synthesis Potential: The compound may be synthesized through various methods, potentially including Friedel-Crafts acylation, highlighting the versatility of synthetic routes available to chemists.
  • Applications in Research: With its unique structural features, 1-(2-pentoxyphenyl)ethanone could serve as an intriguing model compound for studying the effects of substituents on aromatic systems.
  • Role in Materials Science: Compounds like this one are often explored in the development of new materials, including polymers and liquid crystals, due to their potential electronic properties.

Chemical Behavior

The reactivity of 1-(2-pentoxyphenyl)ethanone can be examined through various chemical processes:

  • Reactions with nucleophiles: The carbonyl carbon in the ketone group is highly electrophilic, making it a perfect candidate for nucleophilic addition reactions.
  • Electrophilic aromatic substitution: The presence of the pentoxy group can significantly affect the reactivity of the aromatic ring towards substitution reactions.

In Summary

As a member of the ketone family, 1-(2-pentoxyphenyl)ethanone is a valuable compound not just for theoretical understanding, but also for practical applications in organic synthesis and materials science. Its unique properties make it a fascinating subject for both researchers and students, inviting further exploration and study.

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