220169-88-0

Upstream product

• 1080-05-3 3-(3,5-dimethoxyphenyl)-1-propanol 
• 534-00-9 (S)-2-methylbutyl bromide 
• 125187-47-5 3-(3,5-dimethoxyphenyl)-1-propanal 

Downstream Products

• 220170-13-8 Toluene-4-sulfonic acid (S)-1-[2-(3,5-dimethoxy-phenyl)-ethyl]-3-methyl-pentyl ester 
• 220170-14-9 5-((S)-5-Methyl-heptyl)-benzene-1,3-diol 
• 220169-90-4 (S)-1-(3,5,-dimethoxyphenyl)-5-methylheptane 

Relevant academic research and scientific papers

Synthesis and pharmacology of the isomeric methylheptyl-Δ8-tetrahydrocannabinols

The synthesis of the 3-heptyl, and the eleven isomeric 3-methylheptyl-Δ8-tetrahydrocannabinols (3-7, R and S methyl epimers, and 8) has been carried out. The synthetic approach entailed the synthesis of substituted resorcinols, which were subjected to acid catalyzed condensation with trans-para-menthadienol to provide the Δ8-THC analogue. The 1'-, 2'- and 3'-methylheptyl analogues (3-5) are considerably more potent than Δ8-THC. The 4'-, 5'- and 6'-methylheptyl isomers (6-8) are approximately equal in potency to Δ8-THC. Copyright (C) 1998 Elsevier Science Ltd.