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CAS 1021339-26-3

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N-(2-Chloro-3-hydroxy-4-pyridinyl)-2,2-dimethylpropanamide

Description:
N-(2-Chloro-3-hydroxy-4-pyridinyl)-2,2-dimethylpropanamide is a chemical compound characterized by its unique structural features, which include a pyridine ring substituted with a chlorine atom and a hydroxyl group, alongside a dimethylpropanamide moiety. This compound is typically classified as an amide due to the presence of the carbonyl group (C=O) bonded to a nitrogen atom. The chlorine substitution on the pyridine ring can influence its reactivity and biological activity, potentially enhancing its pharmacological properties. The hydroxyl group contributes to its polarity, which may affect solubility in various solvents. The presence of the dimethylpropanamide structure suggests that it may exhibit steric hindrance, influencing its interactions with biological targets. Overall, this compound may be of interest in medicinal chemistry, particularly in the development of pharmaceuticals, due to its potential biological activity and the presence of functional groups that can participate in various chemical reactions.
Formula:C10H13ClN2O2
InChI:InChI=1S/C10H13ClN2O2/c1-10(2,3)9(15)13-6-4-5-12-8(11)7(6)14/h4-5,14H,1-3H3,(H,12,13,15)
InChI key:InChIKey=DDZBDCPTLSFIME-UHFFFAOYSA-N
SMILES:N(C(C(C)(C)C)=O)C=1C(O)=C(Cl)N=CC1
Synonyms:
  • N-(2-Chloro-3-hydroxy-4-pyridinyl)-2,2-dimethylpropanamide
  • Propanamide, N-(2-chloro-3-hydroxy-4-pyridinyl)-2,2-dimethyl-
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