CAS 1428234-62-1
:2,3-Dichloro-1-methyl-4(1H)-pyridinone
Description:
2,3-Dichloro-1-methyl-4(1H)-pyridinone is a chemical compound characterized by its pyridinone structure, which includes a pyridine ring with a ketone functional group. The presence of two chlorine atoms at the 2 and 3 positions of the ring contributes to its reactivity and potential applications in various chemical processes. The methyl group at the 1 position enhances its lipophilicity, which can influence its solubility and interaction with biological systems. This compound may exhibit biological activity, making it of interest in pharmaceutical research, particularly in the development of agrochemicals or medicinal agents. Its molecular structure suggests potential for hydrogen bonding and other intermolecular interactions, which can affect its physical properties such as melting point, boiling point, and solubility in different solvents. Safety data should be consulted for handling, as halogenated compounds can pose environmental and health risks. Overall, 2,3-Dichloro-1-methyl-4(1H)-pyridinone is a versatile compound with significant implications in both industrial and research settings.
Formula:C6H5Cl2NO
InChI:InChI=1S/C6H5Cl2NO/c1-9-3-2-4(10)5(7)6(9)8/h2-3H,1H3
InChI key:InChIKey=QTAFXQIVANVHMH-UHFFFAOYSA-N
SMILES:ClC1=C(Cl)N(C)C=CC1=O
Synonyms:- 2,3-Dichloro-1-methyl-4(1H)-pyridinone
- 4(1H)-Pyridinone, 2,3-dichloro-1-methyl-
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