
CAS 871325-14-3
:5-Ethyl-2-fluoro-3-pyridinecarboxaldehyde
Description:
5-Ethyl-2-fluoro-3-pyridinecarboxaldehyde is a chemical compound characterized by its pyridine ring structure, which is a six-membered aromatic ring containing one nitrogen atom. The presence of an ethyl group at the 5-position and a fluorine atom at the 2-position contributes to its unique reactivity and properties. The aldehyde functional group at the 3-position is notable for its ability to undergo various chemical reactions, such as oxidation and condensation. This compound is typically a colorless to pale yellow liquid or solid, depending on its state at room temperature. It is soluble in organic solvents, making it useful in organic synthesis and pharmaceutical applications. The fluorine atom can enhance the compound's biological activity and lipophilicity, potentially influencing its interactions in biological systems. As with many organic compounds, safety precautions should be taken when handling it, as it may pose health risks if inhaled or ingested. Overall, 5-Ethyl-2-fluoro-3-pyridinecarboxaldehyde is a versatile compound with applications in medicinal chemistry and material science.
Formula:C8H8FNO
InChI:InChI=1S/C8H8FNO/c1-2-6-3-7(5-11)8(9)10-4-6/h3-5H,2H2,1H3
InChI key:InChIKey=NTZWDMPYAGLTJW-UHFFFAOYSA-N
SMILES:C(=O)C=1C=C(CC)C=NC1F
Synonyms:- 5-Ethyl-2-fluoro-3-pyridinecarboxaldehyde
- 3-Pyridinecarboxaldehyde, 5-ethyl-2-fluoro-
- 5-Ethyl-2-fluoropyridine-3-carboxaldehyde
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