Synthetic Route of 5350-41-4, Because a catalyst decreases the height of the energy barrier, its presence increases the reaction rates of both the forward and the reverse reactions by the same amount.5350-41-4, Name is N,N,N-Trimethyl-1-phenylmethanaminium bromide, molecular formula is C10H16BrN. In a article，once mentioned of 5350-41-4
The photosolvolysis of (-)-1-phenylethyltrimethylammonium iodide in water or methanol is characterised by extensive racemisation accompanied by some net configurational inversion, a result similar to that generally observed in thermal solvolysis via ion-pairs at chiral secondary centres.Recovered quaternary salt from the photolysis in water is only slightly if at all racemised, while likewise there is no observable epimerisation at nitrogen in recovered benzylammonium salts following photolysis in methanol of suitable derivatives of camphidine, trans-decahydroquinoline, and 4-phenylpiperidine.A strong preference for formation of the methyl ether rather than the alcohol is exhibited on either photochemical or thermal solvolysis of 1-p-methoxyphenylethyltrimethylammonium iodide in aqueous methanol, but nucleophile capture ratios during photosolvolysis of simple benzyltrimethylammonium salts in this mixed solvent system are much lower.
We’ll also look at important developments in the pharmaceutical industry because understanding organic chemistry is important in understanding health, medicine, the role of 5350-41-4, and how the biochemistry of the body works.Synthetic Route of 5350-41-4
Reference：
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI