58545-61-2

Upstream product

• 58738-65-1 1,3-dimethoxy-5-[5'-(2H₃)-pentyl]benzene 
• 58545-59-8 C₁₃H₁₈⁽²⁾H₂O₃ 
• 58545-60-1 C₁₃H₁₇⁽²⁾H₂BrO₂ 
• 891-66-7 5-(3,5-Dimethoxy-phenyl)-valeriansaeuremethylester 
• 58545-58-7 (2E,4E)-5-(3,5-Dimethoxy-phenyl)-penta-2,4-dienoic acid methyl ester 
• 111540-03-5 4-(3,5-dimethoxyphenyl)-1-bromobutane 
• 111540-02-4 1-(but-3-en-1-yl)-3,5-dimethoxybenzene 
• 1132-21-4 3,5-dimethoxybenzoic acid 
• 107153-18-4 4-(3,5-dimethoxyphenyl)-1-butanol 
• 504396-91-2 1,3-dimethoxy-5-[3'-(methanesulfonyloxy)-5'-(2H₃)-pentyl]benzene 
• 504396-89-8 1,3-dimethoxy-5-[3'-hydroxy-5'-(2H₃)-pentyl]benzene 
• 125187-47-5 3-(3,5-dimethoxyphenyl)-1-propanal 
• 877-88-3 3,5-dimethoxybenzyl bromide 
• 7311-34-4 3,5-dimethoxybenzaldehdye 

Relevant academic research and scientific papers

Synthesis of side chain specifically deuterated (-)-Δ9-tetrahydrocannabinols

(-)-Δ9-Tetrahydrocannabinols specifically deuterated at the n-pentyl side chain were prepared using the corresponding resorcinols as key intermediates. To obtain the deuterated resorcinols we developed conditions under which no deuterium scramb

A simple and efficient synthesis of 5'-(2H3)olivetol

The title compound 1 was prepared in 13percent overall yield starting from the commercially available and inexpensive 3,5-dimethoxybenzoic acid (4).The n-pentyl side chain was elaborated from cross-coupling reactions between halides.