Simple exploration of (S)-tert-Butyl 3-((methylsulfonyl)oxy)piperidine-1-carboxylate

Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data. Product Details of 940890-90-4, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 940890-90-4, in my other articles.

Chemistry is an experimental science, Product Details of 940890-90-4, and the best way to enjoy it and learn about it is performing experiments.Introducing a new discovery about 940890-90-4, Name is (S)-tert-Butyl 3-((methylsulfonyl)oxy)piperidine-1-carboxylate

Investigation of the effect of varying the 4-anilino and 7-alkoxy groups of 3-quinolinecarbonitriles on the inhibition of Src kinase activity

Several 7-alkoxy-4-anilino-3-quinolinecarbonitriles were synthesized and evaluated for Src kinase inhibitory activity. Optimal inhibition of both Src enzymatic and cellular activity was seen with analogues having a 2,4-dichloro-5-methoxyaniline group at C-4. Compound 18, which has a 1-methylpiperidinemethoxy group at C-7, showed in vivo activity in a xenograft model.

Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data. Product Details of 940890-90-4, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 940890-90-4, in my other articles.

Reference£º
Piperidine – Wikipedia,
Piperidine | C5H22622N – PubChem