166322-69-6

Upstream product

• 68-12-2 N,N-dimethyl-formamide 
• 166322-68-5 3,5-Dimethoxy-2-methylbenzyl chloride 
• 114972-97-3 2,4-dimethoxy-6-methoxymethyltoluene 
• 705-76-0 3,5-dimethoxybenzyl alcohol 
• 166322-67-4 2-(chloromethyl)-4,6-dimethoxy-benzaldehyde 
• 73569-69-4 1-methylmethoxy-3,5-dimethoxybenzene 
• 52344-94-2 methyl 3,5-dimethoxy-2-methylbenzoate 
• 114973-03-4 2,4-dimethoxy-6-(methoxymethyl)benzaldehyde 
• 2150-37-0 methyl 3,5-dimethoxybenzoate 
• 6652-32-0 3,5-dimethoxybenzylchloride 

Downstream Products

• 878480-15-0 2-Chloromethyl-4,6-dimethoxy-3-methyl-benzoic acid 
• 37715-47-2 5,7-Dimethoxy-4-methylisobenzofuran-1(3H)-one 

Relevant academic research and scientific papers

Synthetic study for two 2H-chromenic acids, 8-chlorocannabiorcichromenic acid and mycochromenic acid

Two 2H-chromenes having a fully substituted benzene ring, 8-chlorocannabioreichromene (1) and mycochromenic acid (2), were synthesized by a condensation of salicylaldehydes with isopropylidenemalonate or the thermal cyclization of corresponding propargyl ethers.

An improved synthesis of 5,7-dimethoxy-4-methyl-phthalide, a key intermediate in the synthesis of mycophenolic acid

An efficient synthetic pathway is described for 5,7-dimethoxy-4-methylphthalide, a key intermediate in the synthesis of mycophenolic acid and its analogues. The procedure starts from methyl 3,5-dimethoxybenzoate and involves five simple steps to give phth