CAS 1346691-84-6
:5-(2,6-Difluorophenyl)-3-pyridinecarboxaldehyde
Description:
5-(2,6-Difluorophenyl)-3-pyridinecarboxaldehyde is an organic compound characterized by its unique structure, which includes a pyridine ring and a difluorophenyl group. The presence of the aldehyde functional group (-CHO) indicates that it can participate in various chemical reactions, such as nucleophilic addition and condensation reactions. This compound is likely to exhibit moderate polarity due to the electronegative fluorine atoms and the carbonyl group, influencing its solubility in polar solvents. The difluorophenyl moiety may impart specific electronic properties, potentially affecting its reactivity and interactions with biological targets. Additionally, the compound may have applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to its structural features that can facilitate binding to biological molecules. Its synthesis typically involves multi-step organic reactions, and it may be characterized using techniques such as NMR spectroscopy, mass spectrometry, and infrared spectroscopy to confirm its identity and purity. Overall, 5-(2,6-Difluorophenyl)-3-pyridinecarboxaldehyde represents a valuable compound in the field of organic chemistry.
Formula:C12H7F2NO
InChI:InChI=1S/C12H7F2NO/c13-10-2-1-3-11(14)12(10)9-4-8(7-16)5-15-6-9/h1-7H
InChI key:InChIKey=MXFZRRKIVPFMDN-UHFFFAOYSA-N
SMILES:FC1=C(C(F)=CC=C1)C=2C=C(C=O)C=NC2
Synonyms:- 5-(2,6-Difluorophenyl)-3-pyridinecarboxaldehyde
- 3-Pyridinecarboxaldehyde, 5-(2,6-difluorophenyl)-
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