Interesting facts
Interesting Facts About Phenyl(3-pyridyl)methanone
Pheyl(3-pyridyl)methanone, also known as a compound in the class of ketones, is a fascinating molecule with unique properties and applications in the field of organic chemistry. Below are some intriguing aspects of this compound:
- Structural Importance: This compound features a distinctive structure comprising a phenyl group and a pyridine ring, contributing to its potential reactivity and interactions with other chemical species.
- Biological Significance: Many compounds related to pyridine derivatives have been studied for their biological activities. They may exhibit properties such as antimicrobial, antifungal, and even anti-cancer activities, though further research is necessary for definitive claims regarding phenyl(3-pyridyl)methanone.
- Synthetic Utility: Phenyl(3-pyridyl)methanone can serve as a key intermediate in organic synthesis, enabling the construction of more complex molecules. Such transformations are essential in pharmaceutical development.
- Ligand Capabilities: Compounds like phenyl(3-pyridyl)methanone can act as ligands in coordination chemistry. Their ability to form complexes with metals makes them vital in catalysis and materials science.
- Research Implications: The study of this compound can lead to insights into the reactivity patterns of similar ketones and their derivatives, providing valuable information for chemists aiming to design new compounds with specific functionalities.
To sum up, phenyl(3-pyridyl)methanone is not just an ordinary ketone; it embodies a rich tapestry of structural, biological, and synthetic implications that make it an exciting subject for both researchers and students alike. In the words of a prominent chemist, “The true beauty of chemistry lies in the unexpected potential of simple molecules.”
Synonyms
3-Benzoylpyridine
5424-19-1
Phenyl 3-pyridyl ketone
Methanone, phenyl-3-pyridinyl-
Pyridine, 3-benzoyl-
KETONE, PHENYL 3-PYRIDYL
3-Pyridyl phenyl ketone
EINECS 226-561-3
NSC 13190
Phenyl(3-pyridinyl)methanone
BRN 0120234
NSC-13190
2A1326450X
DTXSID90202591
5-21-08-00572 (Beilstein Handbook Reference)
DTXCID20125082
Methanone, phenyl-3-pyridinyl-(9CI)
226-561-3
inchi=1/c12h9no/c14-12(10-5-2-1-3-6-10)11-7-4-8-13-9-11/h1-9
phenyl(pyridin-3-yl)methanone
3-Benzoyl pyridine
MFCD00006394
UNII-2A1326450X
phenyl-3-pyridyl ketone
Maybridge3_000706
WLN: T6NJ CVR
SCHEMBL125431
Phenyl(3-pyridinyl)methanone #
HMS1433A02
NSC13190
BBL011708
STK802511
AKOS000281712
AC-1855
CS-W019516
FP70247
FS-3267
NB70237
IDI1_012093
SY030036
DB-028366
B0305
NS00033011
EN300-26771
O12042
AC-907/25014300
AC-907/34123031
Q27254455
Z234809824
Solubility of phenyl(3-pyridyl)methanone
Phenyl(3-pyridyl)methanone, with its unique structure featuring both aromatic and heterocyclic components, exhibits intriguing solubility properties. Generally, the solubility of this compound can be influenced by factors such as:
It is often noted that phenyl(3-pyridyl)methanone is more soluble in organic solvents like ethanol, chloroform, and ethyl acetate compared to water. This compound is less soluble in water due to its aromatic nature, which makes it less favorable for interaction with polar water molecules.
As a summation, the solubility of phenyl(3-pyridyl)methanone can be best described by its ability to dissolve in organic solvents while maintaining limited solubility in more polar environments such as water. Understanding these solubility characteristics is essential for applications in both research and industrial contexts.