Brief introduction of 162318-34-5

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.Application of 162318-34-5, you can also check out more blogs about162318-34-5

Application of 162318-34-5, 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. 162318-34-5, Name is 5-Ethynyl-2,2′-bipyridine, molecular formula is C12H8N2. In a Article，once mentioned of 162318-34-5

Copper(l) catalyzed [3+2] cycloaddition reactions between 5-ethynylbipyridine and benzyl, p-methylbenzyl, or m-bromobenzyl azides yields the corresponding l-benzyl-4-(5-bipyridyl)-lH-l,2,3-triazoles 1-3. Reaction between 1-3 and [NEt4J2[Re(CO)3Br3] yields the [l-benzyl-4-(5-bipyridyl)-lH-l,2,3-triaZoIe]Re(CO)3Br complexes 4-6. The Re(CO)3Br complexes of 5- and 6-ethynylbipyridine complexes (78) are prepared in a similar fashion. Cycloaddition reactions between 7 and benzyl azide yields mixtures of 4 and unreacted starting material.

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.Application of 162318-34-5, you can also check out more blogs about162318-34-5

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