1-(2-Pentoxyphenyl)ethanone
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- 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
Identification
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.