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CAS 188577-71-1

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N-(4,5-Dichloro-2-pyridinyl)-2,2-dimethylpropanamide

Description:
N-(4,5-Dichloro-2-pyridinyl)-2,2-dimethylpropanamide, identified by its CAS number 188577-71-1, is a chemical compound that features a pyridine ring substituted with two chlorine atoms at the 4 and 5 positions, contributing to its unique reactivity and biological activity. The presence of the amide functional group indicates that it can participate in hydrogen bonding, which may influence its solubility and interaction with biological targets. The two methyl groups attached to the carbon chain enhance its steric bulk, potentially affecting its pharmacokinetic properties. This compound is often studied for its potential applications in medicinal chemistry, particularly in the development of pharmaceuticals. Its structural characteristics suggest it may exhibit specific interactions with enzymes or receptors, making it a candidate for further research in drug discovery. Additionally, the dichloro substitution may impart unique electronic properties, influencing its reactivity and stability under various conditions. Overall, this compound represents a class of molecules that are of interest in both synthetic and medicinal chemistry.
Formula:C10H12Cl2N2O
InChI:InChI=1S/C10H12Cl2N2O/c1-10(2,3)9(15)14-8-4-6(11)7(12)5-13-8/h4-5H,1-3H3,(H,13,14,15)
InChI key:InChIKey=FRMVYHSNVIYKNI-UHFFFAOYSA-N
SMILES:N(C(C(C)(C)C)=O)C1=CC(Cl)=C(Cl)C=N1
Synonyms:
  • N-(4,5-Dichloropyridin-2-yl)pivalamide
  • N-(4,5-Dichloropyridin-2-yl)-2,2-dimethylpropanamide
  • N-(4,5-Dichloro-2-pyridinyl)-2,2-dimethylpropanamide
  • 4,5-Dichloro-2-(2,2,2-trimethylacetamido)pyridine
  • Propanamide, N-(4,5-dichloro-2-pyridinyl)-2,2-dimethyl-
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