Interesting facts
Interesting Facts About 1-(4-pyridyl)ethanone
1-(4-pyridyl)ethanone, often referred to as a derivative of pyridine, has captivated the interest of chemists due to its unique structural and chemical properties. Here are some intriguing aspects of this compound:
- Structure and Composition: This compound consists of a pyridine ring, which is a six-membered aromatic ring containing five carbon atoms and one nitrogen atom, attached to an ethanone group. This results in a fascinating interplay between the aromatic properties of pyridine and the ketone functionality.
- Reactivity: The presence of the carbonyl group makes 1-(4-pyridyl)ethanone a potential site for various chemical reactions, including nucleophilic additions and condensation reactions, which are valuable in organic synthesis.
- Biological Relevance: Compounds that feature pyridine derivatives, including 1-(4-pyridyl)ethanone, have been studied for their potential pharmacological activities. They may exhibit properties that can be harnessed in medicinal chemistry, leading to the development of new therapeutic agents.
- Complex Formation: This compound can form coordination complexes with transition metals, making it useful in materials science and catalysis. The ability to act as a ligand could open the door to creating novel materials with specific properties.
- Applications: Beyond chemical synthesis, 1-(4-pyridyl)ethanone has applications in various fields including agrochemicals, where it could be used to synthesize herbicides or insecticides.
In summary, the study of 1-(4-pyridyl)ethanone is not just about its molecular structure but also about its diverse applications and contributions to both organic synthesis and biological chemistry. As chemists continue to explore this compound, its full potential may yet unfold, leading to exciting discoveries and innovations.
Synonyms
4-Acetylpyridine
1122-54-9
1-pyridin-4-ylethanone
Ethanone, 1-(4-pyridinyl)-
Methyl 4-pyridyl ketone
Ketone, methyl 4-pyridyl
Pyridine, 4-acetyl-
4-Pyridyl methyl ketone
CCRIS 5954
NSC 111
EINECS 214-350-9
BRN 0107629
AI3-26822
1-(4-PYRIDINYL)ETHANONE
NSC-111
G47437IOW7
PYRIDINE,4-ACETYL
ACETYL PYRIDINE, 4-
DTXSID0022147
5-21-07-00400 (Beilstein Handbook Reference)
gamma-Acetylpyridine
DTXCID402147
214-350-9
inchi=1/c7h7no/c1-6(9)7-2-4-8-5-3-7/h2-5h,1h
4-Acetyl pyridine
1-(pyridin-4-yl)ethan-1-one
MFCD00006433
1-(pyridin-4-yl)ethanone
1-Pyridin-4-yl-ethanone
1-(4-pyridyl)ethanone
UNII-G47437IOW7
4-Acetyl-pyridine
.gamma.-Acetylpyridine
4-Acetylpyridine, 97%
WLN: T6NJ DV1
1-(pyridin-4-yl)-ethanone
SCHEMBL55235
1-(4-Pyridinyl)ethanone #
METHYL 4-PYRIDYLKETONE
CHEMBL445953
NSC111
HY-Y0179
STL185607
AKOS000119796
AB00760
AC-8358
CS-W008727
FG-0441
SY005519
DB-012784
A0113
NS00021527
EN300-17993
4-Acetylpyridine, Vetec(TM) reagent grade, 97%
Q27278737
F0001-0269
Solubility of 1-(4-pyridyl)ethanone
The solubility of 1-(4-pyridyl)ethanone, also known as 4-pyridylacetone, can be influenced by various factors. Here are some key points to consider:
In summary, the solubility of 1-(4-pyridyl)ethanone can be described as relatively favorable in polar solvents, making it useful for numerous applications in organic synthesis and other chemical processes. As one explores its solubility, it is essential to consider the specific solvent and the experimental conditions applied.