CAS 131418-17-2
:2-chloro-N-ethyl-pyridine-4-carboxamide
Description:
2-Chloro-N-ethyl-pyridine-4-carboxamide is a chemical compound characterized by its pyridine ring structure, which is a six-membered aromatic ring containing one nitrogen atom. The presence of a chloro group at the second position and an ethyl group attached to the nitrogen atom contributes to its unique properties. This compound features a carboxamide functional group, which enhances its solubility in polar solvents and may influence its reactivity. Typically, compounds like this can exhibit biological activity, making them of interest in pharmaceutical research. The molecular structure suggests potential interactions with biological targets, possibly affecting enzyme activity or receptor binding. Additionally, the presence of the chloro substituent may impart specific electronic and steric effects, influencing the compound's overall stability and reactivity. Safety and handling considerations are essential, as halogenated compounds can pose environmental and health risks. Overall, 2-chloro-N-ethyl-pyridine-4-carboxamide represents a class of compounds that may have significant applications in medicinal chemistry and related fields.
Formula:C8H9ClN2O
InChI:InChI=1/C8H9ClN2O/c1-2-10-8(12)6-3-4-11-7(9)5-6/h3-5H,2H2,1H3,(H,10,12)
SMILES:CCN=C(c1ccnc(c1)Cl)O
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Found 2 products.
2-Chloro-N-ethylpyridine-4-carboxamide
CAS:<p>Versatile small molecule scaffold</p>Formula:C8H9ClN2OPurity:Min. 95%Molecular weight:184.62 g/mol

