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CAS 898561-61-0

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

Description:
N-(4-Chloro-3-iodo-2-pyridinyl)-2,2-dimethylpropanamide is a chemical compound characterized by its unique structure, which includes a pyridine ring substituted with chlorine and iodine atoms, contributing to its reactivity and potential biological activity. The presence of the amide functional group indicates that it can participate in hydrogen bonding, influencing its solubility and interaction with biological targets. The bulky 2,2-dimethylpropanamide moiety enhances steric hindrance, which may affect the compound's pharmacokinetics and binding affinity in biological systems. This compound is likely to exhibit specific properties such as lipophilicity due to its hydrophobic regions, which can impact its absorption and distribution in living organisms. Additionally, the halogen substituents (chlorine and iodine) can impart unique electronic characteristics, potentially enhancing its reactivity in certain chemical reactions. Overall, this compound may be of interest in medicinal chemistry and drug development, particularly in the context of targeting specific biological pathways or receptors.
Formula:C10H12ClIN2O
InChI:InChI=1S/C10H12ClIN2O/c1-10(2,3)9(15)14-8-7(12)6(11)4-5-13-8/h4-5H,1-3H3,(H,13,14,15)
InChI key:InChIKey=IOIUSHNLFZWBBP-UHFFFAOYSA-N
SMILES:N(C(C(C)(C)C)=O)C1=C(I)C(Cl)=CC=N1
Synonyms:
  • N-(4-Chloro-3-iodo-2-pyridinyl)-2,2-dimethylpropanamide
  • Propanamide, N-(4-chloro-3-iodo-2-pyridinyl)-2,2-dimethyl-
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