71226-16-9

Upstream product

• 7147-44-6 1-(2-chlorophenyl)ethanone oxime 
• 106-89-8 epichlorohydrin 
• 2142-68-9 1-(2-chlorophenyl)ethanone 

Downstream Products

• 89331-59-9 N-(2-{3-[1-(2-Chloro-phenyl)-eth-(Z)-ylideneaminooxy]-2-hydroxy-propylamino}-ethyl)-isobutyramide; compound with oxalic acid 
• 89331-57-7 1-(2-Chloro-phenyl)-ethanone O-[3-(2-benzylsulfanyl-ethylamino)-2-hydroxy-propyl]-oxime; hydrochloride 
• 89331-55-5 1-(2-Chloro-phenyl)-ethanone O-[2-hydroxy-3-(1-phenyl-propylamino)-propyl]-oxime; hydrochloride 
• 89331-58-8 1-(2-Chloro-phenyl)-ethanone O-{3-[2-(3,4-dimethoxy-phenyl)-ethylamino]-2-hydroxy-propyl}-oxime; hydrochloride 
• 89331-56-6 1-(2-Chloro-phenyl)-ethanone O-[2-hydroxy-3-(1-methyl-3-phenyl-propylamino)-propyl]-oxime; hydrochloride 

Relevant academic research and scientific papers

Synthesis of β-blocking oximes. Influence of terminal amine on β-selectivity

Three series of oximinopropanolamine derivatives in which the terminal nitrogen has been substituted by various arylalkyl groups were synthesized. The beta-adrenergic blocking activity of the 21 compounds was determined in vitro on the guinea-pig. The structure-activity relationship is discussed.