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2'-Methylacetophenone

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Identification
Molecular formula
C10H12O
CAS number
577-16-2
IUPAC name
1-(2-ethylphenyl)ethanone
State
State

At room temperature, 2'-Methylacetophenone is a liquid. Its state is affected by its aromatic ketone structure, which imparts certain solvent-like characteristics while maintaining a relatively low viscosity.

Melting point (Celsius)
-19.00
Melting point (Kelvin)
254.15
Boiling point (Celsius)
244.00
Boiling point (Kelvin)
517.15
General information
Molecular weight
148.20g/mol
Molar mass
148.2010g/mol
Density
1.0068g/cm3
Appearence

2'-Methylacetophenone is a colorless to pale yellow liquid characterized by its aromatic ketone scent. It is a derivative of acetophenone with the key distinction being the addition of a methyl group on the aromatic ring, which influences the compound's chemical behavior and olfactory properties.

Comment on solubility

Solubility of 1-(2-ethylphenyl)ethanone

The solubility of 1-(2-ethylphenyl)ethanone, a compound with the formula C10H12O, is an interesting topic for discussion. This organic compound, commonly known as 2-ethylacetophenone, is a colorless liquid with a characteristic odor, and its solubility behavior can be influenced by various factors. Here are some key points to consider:

  • Polar vs. Non-Polar Solvents: 1-(2-ethylphenyl)ethanone tends to be more soluble in non-polar solvents like hexane or toluene due to its relatively non-polar aromatic structure. However, it shows limited solubility in polar solvents such as water.
  • Temperature Dependency: Solubility can vary significantly with temperature. As temperature increases, generally, the solubility in organic solvents tends to increase as well, due to enhanced molecular interactions.
  • Concentration Effects: At higher concentrations, the solubility may reach a limit, beyond which the compound may not dissolve further, leading to precipitation or formation of a separate phase.

In summary, while 1-(2-ethylphenyl)ethanone can dissolve readily in non-polar organic solvents, its solubility in polar solvents remains quite restricted. Understanding these solubility characteristics is crucial for various applications in organic synthesis and material chemistry.

Interesting facts

Interesting Facts about 1-(2-ethylphenyl)ethanone

1-(2-ethylphenyl)ethanone, also known as a ketone, is a fascinating compound that showcases the intriguing world of organic chemistry. This compound not only holds significant industrial value but also contributes to the understanding of complex chemical structures. Here are some interesting insights into this unique substance:

  • Structural Significance: The compound features a ketone functional group, characterized by a carbonyl group (C=O) bonded to two carbon atoms. This allows it to participate in various chemical reactions, facilitating its use in organic synthesis.
  • Applications: This compound is often used in the production of fragrances and flavorings due to its pleasant aroma. It also plays a role in the synthesis of other more complex organic compounds, thus highlighting its importance in chemical research and industry.
  • Biological Activity: Several studies have indicated that ketones can exhibit noteworthy biological activities. While 1-(2-ethylphenyl)ethanone itself may not be the focus of extensive biological research, its derivatives could potentially yield insights into pharmaceutical applications.
  • Synthesis Pathways: The synthesis of 1-(2-ethylphenyl)ethanone can be achieved through various methods, including Friedel-Crafts acylation. This process exemplifies the beauty of organic transformations and showcases the flexibility of ketone chemistry.
  • Analytical Chemistry: Ketones like this compound can be analyzed using techniques such as Gas Chromatography-Mass Spectrometry (GC-MS), enabling chemists to assess purity, structural confirmation, and concentration, which are crucial for research and industrial applications.

The study of 1-(2-ethylphenyl)ethanone emphasizes the significance of ketones in both industrial applications and research advancements. As the field of organic chemistry evolves, understanding such compounds lays the groundwork for innovative discoveries in various domains.

Synonyms
2142-64-5
2'-ETHYLACETOPHENONE
DTXSID20175688
DTXCID1098179
vlilfbzivhdkij-uhfffaoysa-n
1-(2-ethylphenyl)ethanone
1-(2-ethylphenyl)ethan-1-one
Ethanone, 1-(ethylphenyl)-
2-ethylacetophenone
1-(2-ethyl-phenyl)-ethanone
o-Ethylaceto-phenone
SCHEMBL254888
CAA14264
AKOS017516397
AS-58375
CS-0308287
A10857
EN300-113955