The important role of 2390-68-3

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.Synthetic Route of 2390-68-3, you can also check out more blogs about2390-68-3

Synthetic Route of 2390-68-3, A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 2390-68-3, Name is N-Decyl-N,N-dimethyldecan-1-aminium bromide, molecular formula is C22H48BrN. In a Article,once mentioned of 2390-68-3

A catalyst-free condensation reaction of alpha,beta-Unsaturated ketones and sodium sulfide in CH3CN-H2O mixture (1:1) was established to prepare a variety of polysubstituted tetrahydrothiopyrans in good to excellent yields. The obtained tetrahydrothiopyrans were oxidized with MCPBA to the corresponding sulfoxides in good yields. The present research is the first report on synthesis of polysubstituted tetrahydrothiopyran sulfoxides.

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.Synthetic Route of 2390-68-3, you can also check out more blogs about2390-68-3

Reference:
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI