CAS 1142191-76-1
:N-(2-Chloro-6-formyl-3-pyridinyl)-2,2-dimethylpropanamide
Description:
N-(2-Chloro-6-formyl-3-pyridinyl)-2,2-dimethylpropanamide is a chemical compound characterized by its unique structural features, which include a pyridine ring substituted with a chloro and an aldehyde functional group, along with a dimethylpropanamide moiety. This compound is likely to exhibit properties typical of amides, such as moderate polarity and the ability to participate in hydrogen bonding due to the presence of the amide functional group. The chloro substituent may influence its reactivity and solubility in various solvents. Additionally, the presence of the formyl group suggests potential reactivity in condensation reactions or as a precursor for further synthetic transformations. The compound's molecular structure indicates potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to the bioactive nature of pyridine derivatives. Overall, the characteristics of this compound make it a subject of interest for further research in organic synthesis and drug development.
Formula:C11H13ClN2O2
InChI:InChI=1S/C11H13ClN2O2/c1-11(2,3)10(16)14-8-5-4-7(6-15)13-9(8)12/h4-6H,1-3H3,(H,14,16)
InChI key:InChIKey=LZRCTDNVNSXRKD-UHFFFAOYSA-N
SMILES:N(C(C(C)(C)C)=O)C1=C(Cl)N=C(C=O)C=C1
Synonyms:- Propanamide, N-(2-chloro-6-formyl-3-pyridinyl)-2,2-dimethyl-
- N-(2-Chloro-6-formyl-3-pyridinyl)-2,2-dimethylpropanamide
- N-(2-Chloro-6-formylpyridin-3-yl)pivalamide
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