Skip to main content

1-(2-Pentoxyphenyl)ethanone

ADVERTISEMENT
Identification
Molecular formula
C13H18O2
CAS number
37643-29-7
IUPAC name
1-(2-pentoxyphenyl)ethanone
State
State

At room temperature, 1-(2-Pentoxyphenyl)ethanone is in a liquid state. It is somewhat volatile under ambient conditions, given its aromatic characteristics.

Melting point (Celsius)
-30.00
Melting point (Kelvin)
243.15
Boiling point (Celsius)
283.00
Boiling point (Kelvin)
556.15
General information
Molecular weight
190.25g/mol
Molar mass
190.2500g/mol
Density
1.0120g/cm3
Appearence

1-(2-Pentoxyphenyl)ethanone appears as a colorless to light yellow liquid. Its aromatic structure imparts a characteristic odor, which is mild and sweet.

Comment on solubility

Solubility of 1-(2-pentoxyphenyl)ethanone

The solubility of 1-(2-pentoxyphenyl)ethanone in various solvents can provide valuable insights into its chemical behavior and applications. This compound, with the chemical formula C13H18O, exhibits distinct solubility characteristics:

  • Polar Solvents: The presence of the ether functional group in its structure suggests that 1-(2-pentoxyphenyl)ethanone may have moderate solubility in polar solvents, such as water and alcohols, although the overall solubility might be limited due to its hydrophobic pentoxy group.
  • Non-Polar Solvents: It is expected to be more soluble in non-polar solvents like hexane or toluene, as its hydrophobic characteristics are better accommodated in these environments.
  • Temperature Dependence: Like many organic compounds, its solubility may increase with temperature, thus expanding its applicability in various chemical processes.

To summarize, 1-(2-pentoxyphenyl)ethanone displays variable solubility depending on the solvent's polarity. Its ability to dissolve in both polar and non-polar media can be advantageous for tasks ranging from synthesis to formulation in chemical industries.

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.

Synonyms
2'-Pentyloxyacetophenone
7191-39-1
2-n-Amyloxyacetophenone
ACETOPHENONE, 2'-(PENTYLOXY)-
Ethanone, 1-(2-(pentyloxy)phenyl)-
18AZ4U6F78
2'-(Pentyloxy)acetophenone
1-(2-pentoxyphenyl)ethanone
BRN 2615073
2'-n-Pentoxyacetophenone
EINECS 230-556-1
UNII-18AZ4U6F78
SCHEMBL524256
DTXSID80222162
DHDSALKEOLDSSE-UHFFFAOYSA-N
PBA76550
AKOS000203250
NS00037303
Q27251990