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3'-Ethylacetophenone

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Identification
Molecular formula
C10H12O
CAS number
89897-64-5
IUPAC name
1-(3-ethylphenyl)ethanone
State
State

At room temperature, 3'-Ethylacetophenone is a liquid.

Melting point (Celsius)
-30.00
Melting point (Kelvin)
243.15
Boiling point (Celsius)
229.00
Boiling point (Kelvin)
502.15
General information
Molecular weight
148.20g/mol
Molar mass
148.2020g/mol
Density
0.9983g/cm3
Appearence

3'-Ethylacetophenone appears as a colorless to pale yellow liquid.

Comment on solubility

Solubility of 1-(3-ethylphenyl)ethanone

The solubility of 1-(3-ethylphenyl)ethanone, a ketone compound, can be influenced by several factors, primarily its molecular structure and interactions with solvents. Here are some key points regarding its solubility:

  • Polarity: 1-(3-ethylphenyl)ethanone contains both a hydrophobic aromatic ring and a more polar carbonyl group. This polarity affects its solubility in various solvents.
  • Solvent Compatibility: The compound is likely to be more soluble in organic solvents such as ethanol, acetone, and chloroform rather than in water due to its hydrophobic characteristics.
  • Temperature Influence: As with many organic compounds, increased temperature can lead to enhanced solubility. Higher temperatures typically help dissolve solids more readily in liquids.

In general, while the exact solubility can vary based on environmental conditions, it is safe to conclude that 1-(3-ethylphenyl)ethanone is more soluble in non-polar and weakly polar solvents than in polar solvents. This behavior is typical for many ketones, reflective of their structural attributes.

Interesting facts

Exploring 1-(3-ethylphenyl)ethanone

1-(3-ethylphenyl)ethanone, a fascinating organic compound, belongs to the class of ketones. This compound exhibits intriguing properties that make it a subject of study in various scientific fields. Here are some noteworthy aspects:

  • Key Applications: This compound is often utilized in the synthesis of various pharmaceuticals and fragrances, highlighting its significance in both the chemical industry and perfume formulation.
  • Chemical Behavior: As a ketone, 1-(3-ethylphenyl)ethanone possesses a carbonyl group (C=O), which contributes to its reactivity and the formation of diverse derivatives. This feature is essential for understanding its behavior in organic reactions.
  • Historical Context: Ketones have played a pivotal role in the development of organic chemistry. The study of compounds like 1-(3-ethylphenyl)ethanone provides insight into the evolution of synthetic methodologies.
  • Structure and Symmetry: The arrangement of its ethyl group on the aromatic ring influences its spatial conformation, which can affect its physical and chemical properties, making it an exciting topic for chemists interested in molecular geometry.

In the words of renowned chemist Linus Pauling, "Chemistry is the study of the properties of substances and the changes they undergo." 1-(3-ethylphenyl)ethanone is a perfect example of this principle in action!

Overall, the study of 1-(3-ethylphenyl)ethanone not only enhances our understanding of ketones but also opens doors to various applications and implications in modern chemistry.

Synonyms
3-ETHYLACETOPHENONE
22699-70-3
1-(3-Ethylphenyl)ethan-1-one
m-Ethylacetophenone
Acetophenone, 3-ethyl-
DTXSID20177223
RefChem:552425
DTXCID2099714
995-220-5
1-(3-Ethylphenyl)ethanone
3'-ETHYLACETOPHENONE
Ethanone,1-(3-ethylphenyl)-
MFCD00009660
Ethanone, 1-(3-ethylphenyl)-
1-acetyl-3-ethylbenzene
methylacetophenon
m-Acetyl ethyl benzene
SCHEMBL334537
SCHEMBL2541572
SCHEMBL4324735
CHEBI:194773
BBL102901
CL9636
SBB064783
STL556710
AKOS006228241
FE67733
PS-5477
SY239126
DB-045969
CS-0207257
NS00010756
3 inverted exclamation mark -Ethylacetophenone
EN300-1827755
699E703
F226299