Interesting facts
Interesting Facts about 1-(4-acetylphenyl)ethanone
1-(4-acetylphenyl)ethanone, also known as 4-acetylphenylacetone, is a fascinating compound that exhibits a range of intriguing properties and uses. Here are some interesting facts that highlight its importance and appeal:
- Chemical Structure: This compound features a ketone functional group combined with a phenyl ring. The presence of the acetyl group contributes to its reactivity and versatility in various chemical reactions.
- Synthesis: 1-(4-acetylphenyl)ethanone can be synthesized through various methods, often involving the Friedel-Crafts acylation of acetophenone, making it an excellent subject for students exploring organic synthesis techniques.
- Applications: Its applications are broad and noteworthy. Primarily, it serves as a precursor in the manufacture of pharmaceuticals, flavorings, and fragrances. It can be explored for potential uses in the pharmaceutical industry for synthesizing advanced drug candidates.
- Visual Appearance: While the specific appearance of the compound is not discussed, it typically exists in a form that is conducive to interaction in a laboratory environment, making it easy to handle and incorporate into various chemical processes.
- Interesting Reactions: Given its structure, it can participate in various reactions, such as nucleophilic addition and condensation reactions, offering a rich ground for experimental chemistry.
- Research Potential: Ongoing research is being conducted on derivatives of 1-(4-acetylphenyl)ethanone, which may reveal novel biological activities, emphasizing the compound's significance in medicinal chemistry.
In summary, 1-(4-acetylphenyl)ethanone is more than just a chemical; it signifies the intersection between industrial application and academic study, prompting curiosity and encouraging further investigation in the realm of organic chemistry.
Synonyms
1,4-Diacetylbenzene
1009-61-6
p-Acetylacetophenone
p-Diacetylbenzene
Ethanone, 1,1'-(1,4-phenylene)bis-
Benzene, p-diacetyl-
DTXSID7021657
EINECS 213-769-4
NSC 295548
DTXCID601657
pDiacetylbenzene
pAcetylacetophenone
Benzene, pdiacetyl
Benzene, pdiacetyl (8CI)
Benzene, p-diacetyl-(8CI)
Ethanone, 1,1'(1,4phenylene)bis
213-769-4
1,1'-(1,4-phenylene)diethanone
1-(4-acetylphenyl)ethanone
1-(4-Acetylphenyl)ethan-1-one
4'-Acetylacetophenone
MFCD00008750
1-(4-Acetyl-phenyl)-ethanone
1,1-(1,4-Phenylene)bis-ethanone
1,1'-(1,4-phenylene)bis-Ethanone
NSC-295548
4-Acetylacetophenone
1,4-diacetyl benzene
WM5GGF7BQ6
1-(4-acetylphenyl)ethanon
SCHEMBL50646
P-ACETHYL ACETOPHENONE
1,4-Diacetylbenzene, 99%
1-(4-acetylphenyl)-ethanone
CHEMBL3186189
ALBB-035799
Ethanone,1'-(1,4-phenylene)bis-
Tox21_201219
NSC295548
AKOS003628600
FD69972
NCGC00248961-01
NCGC00258771-01
AS-61744
SY017824
CAS-1009-61-6
1,1'-(1,4-Phenylene)bis(ethan-1-one)
CS-0155100
D0066
NS00010678
Q63399973
InChI=1/C10H10O2/c1-7(11)9-3-5-10(6-4-9)8(2)12/h3-6H,1-2H
Solubility of 1-(4-acetylphenyl)ethanone
1-(4-acetylphenyl)ethanone, also known as 4-acetylacetophenone, exhibits interesting solubility characteristics that are crucial for its applications in various chemical processes.
This compound, which features a ketone functional group, is generally regarded as being:
The solubility behavior can be influenced by several factors, including:
When considering solvents for applications or reactions involving 1(4-acetylphenyl)ethanone, it is beneficial to choose polar solvents to maximize dissolution. As stated, "the choice of solvent is pivotal in determining the practical applicability of a compound." Thus, understanding the solubility profile is essential for laboratory practices and industrial applications alike.