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4'-Isopropylacetophenone

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Identification
Molecular formula
C11H14O
CAS number
645-59-0
IUPAC name
1-(4-isopropylphenyl)ethanone
State
State

At room temperature, 4'-Isopropylacetophenone is typically a liquid.

Melting point (Celsius)
-19.00
Melting point (Kelvin)
254.15
Boiling point (Celsius)
248.00
Boiling point (Kelvin)
521.15
General information
Molecular weight
148.20g/mol
Molar mass
148.2010g/mol
Density
0.9495g/cm3
Appearence

4'-Isopropylacetophenone is a colorless to pale yellow liquid. It is characterized by its distinct aromatic odor.

Comment on solubility

Solubility of 1-(4-isopropylphenyl)ethanone

1-(4-isopropylphenyl)ethanone, also known as p-isopropylacetophenone, showcases interesting solubility characteristics that are significant for various applications. This compound, classified as an aromatic ketone, presents several noteworthy attributes:

  • Solvent Compatibility: 1-(4-isopropylphenyl)ethanone is moderately soluble in organic solvents such as ethanol, methanol, and acetone, which makes it useful in synthetic organic chemistry.
  • Water Solubility: The solubility in water is generally low; thus, it is considered hydrophobic in nature. This is typical for many aromatic compounds.
  • Temperature Dependency: The solubility can vary with temperature, increasing at higher temperatures due to enhanced molecular interactions.
  • Effect of Structural Features: The bulky isopropyl group contributes to the hydrophobic character, impacting the overall solubility in polar solvents.

In summary, one can observe that the solubility of 1-(4-isopropylphenyl)ethanone is influenced by its molecular structure and the nature of the solvent. Such characteristics make it a useful compound in various chemical processes where solvent choice is critical.

Interesting facts

Interesting Facts about 1-(4-isopropylphenyl)ethanone

1-(4-isopropylphenyl)ethanone, commonly known as isopropyl phenyl ketone, is an intriguing compound with various applications in both industrial and academic settings. Here are some captivating details:

  • Chemical Structure: This compound features a ketone functionality characterized by a carbonyl group (C=O) directly attached to a phenyl ring that is further substituted with an isopropyl group. This unique arrangement significantly influences its reactivity and properties.
  • Applications: 1-(4-isopropylphenyl)ethanone is widely utilized in the chemical industry as an intermediate in the synthesis of various organic compounds. It plays a vital role in the production of fragrances and flavorings due to its aromatic structure.
  • Photoinitiator: Interestingly, this compound is also employed as a photoinitiator in polymer chemistry. When exposed to UV light, it initiates polymerization reactions, making it essential for producing plastics and coatings.
  • Chemical Behavior: The presence of the isopropyl group enhances the steric hindrance around the carbonyl, affecting the stability and reactivity of the ketone. Such variations can lead to unique reaction pathways, making it an essential study subject for chemical kinetics.
  • Research Insights: Academically, researchers often investigate compounds like 1-(4-isopropylphenyl)ethanone to understand the behavior of substituted aromatic ketones. They provide insights into electronic effects and structure-activity relationships within organic chemistry.
  • Safety Precautions: As with many organic compounds, handling 1-(4-isopropylphenyl)ethanone requires caution. Researchers must follow proper safety protocols, including the use of protective gear and working in well-ventilated areas to mitigate exposure risks.

Overall, 1-(4-isopropylphenyl)ethanone presents a fascinating field of study with numerous implications in both practical applications and theoretical research. Its diverse roles in chemistry exemplify the importance of understanding compound functionality and structure.

Synonyms
4'-Isopropylacetophenone
645-13-6
4-ISOPROPYLACETOPHENONE
Cuminone
p-Isopropylacetophenone
Ethanone, 1-[4-(1-methylethyl)phenyl]-
Acetophenone, 4'-isopropyl-
Methyl p-isopropylphenyl ketone
Acetylcumene, p-
FEMA No. 2927
p-Acetylcumene
Isopropylacetylbenzene, p-
1-(4-(1-Methylethyl)phenyl)ethanone
742ZKZ2A6D
1-[4-(propan-2-yl)phenyl]ethan-1-one
1-(4-(1-Methylethyl)phenyl)ethan-1-one
1-[4-(1-Methylethyl)phenyl]ethan-1-one
Ethanone, 1-(4-(1-methylethyl)phenyl)-
p-Isopropylacetylbenzene
NSC 9165
NSC-9165
EINECS 211-433-1
AI3-15527
P-ISOPROPYL ACETOPHENONE
DTXSID0052330
P-ISOPROPYLACETOPHENONE [FHFI]
1-[4-(1-methylethyl)phenyl]Ethanone
1-(4-(propan-2-yl)phenyl)ethan-1-one
DTXCID0030902
Acetophenone, 4'-isopropyl-(8CI)
Ethanone, 1-4-(1-methylethyl)phenyl-
211-433-1
1-(4-Isopropylphenyl)ethanone
1-(4-propan-2-ylphenyl)ethanone
MFCD00048297
(4-Isopropylphenyl)ethanone
1-[4-(propan-2-yl)phenyl]ethanone
1-(4-Isopropylphenyl)ethanone (4-Isopropylacetophenone)
1-(4-(1-Methylethyl)phenyl)-Ethanone
1-[4-(1-Methylethyl)phenyl]-Ethanone
1-(4-Isopropylphenyl)ethanone; 4-Isopropylacetophenone
UNII-742ZKZ2A6D
NSC9165
4-isopropylacetophenon
Methyl p-cumyl ketone
p-iso-propylacetophenone
4\'-Isopropylacetophenone
4'-Isopropyl-Acetophenone
4(2)-Isopropylacetophenone
SCHEMBL182327
FEMA 2927
1-(4-isopropyl-phenyl)-ethanone
1-(4-Isopropylphenyl)ethanone #
AAA64513
STR06928
STK397403
4'-Isopropylacetophenone, AldrichCPR
Acetophenone, 4'-isopropyl- (8CI)
AKOS000296233
PS-4575
SY012990
DB-073506
1-[4-(1-Methylethyl)phenyl]ethanone, 9CI
I0570
NS00008450
EN300-07967
H11892
4 inverted exclamation mark -Isopropylacetophenone
SR-01000944848
SR-01000944848-1
Q27266227
Z56963407
F0001-1746
1-[4-(Prop-2-yl)phenyl]ethan-1-one, 4'-(Prop-2-yl)acetophenone