930598-01-9

Upstream product

• 77-78-1 dimethyl sulfate 
• 930597-96-9 dimethyl [1-(2,6-dimethoxy-4-pentylphenyl)allyl]malonate 
• 930598-00-8 3-(2,6-dimethoxy-4-pentyl-phenyl)-pent-4-enoic acid methyl ester 
• 154106-15-7 3-methylbut-3-en-1-yl trifluoromethanesulphonate 

Downstream Products

• 930598-04-2 2-(2,6-dimethoxy-4-pentylphenyl)-4-methyl-cyclohex-3-enecarboxylic acid methyl ester 
• 930597-95-8 methyl (1R,2R)-2',6'-dimethoxy-5-methyl-4'-pentyl-1,2,3,4-tetrahydro-[1,1'-biphenyl]-2-carboxylate 
• 930598-05-3 2-[2-(2,6-dimethoxy-4-pentylphenyl)-4-methyl-cyclohex-3-enyl]-2-propanol 
• 1972-08-3 dronabinol 
• 36403-68-6 D1,2-Tetrahydrocannabinol methyl ether 
• 488787-51-5 (3R,4R)-3-[(2-hydroxy-6-methoxy-4-pentyl)phenyl]-1-methyl-4-[(1-methyl-1-triethylsilyloxy)ethyl]-1-cyclohexene 

Relevant academic research and scientific papers

Synthesis of (-)-Δ9-trans-tetrahydrocannabinol: Stereocontrol via mo-catalyzed asymmetric allylic alkylation reaction

(Chemical Equation Presented) Δ9-THC is synthesized in enantiomericaly pure form, where all of the stereochemistry is derived from the molybdenum-catalyzed asymmetric alkylation reaction of the extremely sterically congested bis-ortho-substitut