57168-46-4

Upstream product

• 31374-71-7 3,4,5-triethoxybenzoic acid ethyl ester 
• 39727-75-8 3,4,5-triethoxybenzyl alcohol 
• 143-33-9 sodium cyanide 
• 86603-79-4 3,4,5-triethoxybenzyl chloride 

Downstream Products

• 90109-63-0 3,4,5-triethoxyphenethylamine 

Relevant academic research and scientific papers

Sulfur Analogues of Psychotomimetic Agents. 3. Ethyl Homologues of Mescaline and Their Monothio Analogues

All possible monothio analogues of the mono-, di-, and triethoxy homologues of mescaline have been synthesized and pharmacologically evaluated in man.Modifications at the ring position para to the ethylamine chain, either with a sulfur atom, a longer alkyl chain, or both, lead to compounds of high central nervous system activity.The 4-n-propoxy and 4-n-butoxy homologues and their corresponding 4-thio analogues were also synthesized and pharmacologically evaluated.The propyl homologues retain high potency, but a butyl group (either with or without a sulfur atom) leads to a decrease in activity.The m-ethyl or m-thio analogues retain some central action but the diethoxy and especially the triethoxy homologues are relatively inactive as psychotomimetic drugs.