Downstream Synthetic Route Of 23794-15-2

In some applications, this compound(23794-15-2)Reference of 1-(2-chloropyridine-4-yl)ethanone is unique.If you want to know more details about this compound, you can contact with the author or consult more relevant literature.

Alvey, Luke; Prado, Soizic; Huteau, Valerie; Saint-Joanis, Brigitte; Michel, Sylvie; Koch, Michel; Cole, Stewart T.; Tillequin, Francois; Janin, Yves L. published an article about the compound: 1-(2-chloropyridine-4-yl)ethanone( cas:23794-15-2,SMILESS:CC(=O)C1=CC(Cl)=NC=C1 ).Reference of 1-(2-chloropyridine-4-yl)ethanone. Aromatic heterocyclic compounds can be classified according to the number of heteroatoms or the size of the ring. The authors also want to convey more information about this compound (cas:23794-15-2) through the article.

From the structure of 3,3-dimethyl-3H-benzofuro[3,2-f][1]-benzopyran, a selective in vitro inhibitor of mycobacterial growth, a structure-activity relationship investigation has been undertaken. Reported here are the results on the use of [2+3] cycloadditions between 2-formylbenzoquinone and various enol derivatives to give various 4-formyl-5-hydroxy benzofurans. In the next step, an ytterbium triflate-catalyzed reaction with 2-methylpropene allowed the preparation of various original furo[3,2-f]chromenes derivatives Their biol. evaluation on the growth of Mycobacterium smegmatis as well as Mycobacterium tuberculosis pointed out that some analogs were four times more active than the initial hit.

In some applications, this compound(23794-15-2)Reference of 1-(2-chloropyridine-4-yl)ethanone is unique.If you want to know more details about this compound, you can contact with the author or consult more relevant literature.

Reference:
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