69336-17-0

Upstream product

• 4707-47-5 2,4-dihydroxy-3,6-dimethyl-benzoic acid methyl ester 
• 100-39-0 benzyl bromide 

Downstream Products

• 58062-00-3 methyl 4-benzyloxy-2-methoxy-3,6-dimethylbenzoate 
• 56410-32-3 4-benzyloxy-2-hydroxy-3,6-dimethylbenzoic acid 
• 17636-16-7 barbatic acid 
• 56410-44-7 benzyl 2-hydroxy-4-((2-hydroxy-4-methoxy-3,6-dimethylbenzoyl)oxy)-3,6-dimethyl benzoate 
• 56410-30-1 benzyl 2,4-dihydroxy-3,6-dimethylbenzoate 
• 4707-46-4 2,4-dihydroxy-3,6-dimethylbenzoic acid 
• 78023-68-4 methyl 4-benzyloxy-3-(2,4-bisbenzyloxy-3,6-dimethylbenzoyl)-6-methoxy-2,5-dimethylbenzoate 
• 78023-69-5 methyl 3-(2,4-dihydroxy-3,6-dimethylbenzoyl)-4-hydroxy-6-methoxy-2,5-dimethylbenzoate 
• 78023-67-3 2-benzyloxy-5-methoxycarbonyl-4-methoxy-3,6-dimethylbenzoic acid 
• 78023-66-2 methyl 4-benzyloxy-3-formyl-6-methoxy-2,5-dimethylbenzoate 
• 78023-65-1 methyl 3-formyl-4-hydroxy-6-methoxy-2,5-dimethylbenzoate 
• 34874-75-4 methyl 4-hydroxy-2-methoxy-3,6-dimethylbenzoate 

Relevant academic research and scientific papers

Depsidone Synthesis. Part 19. Some β-Orcinol Depsidones

The synthesis of the lichen depsidones 3,8-dihydroxy-1,4,6,9-tetramethyl-11-oxo-11H-dibenzo-dioxepin-7-carboxylic acid (hypoprotocetraric acid) (4), 8-hydroxy-3-methoxy-1,4,6,9-tetramethyl-11-oxo-11H-dibenzodioxepin-7-carboxylic acid (

Synthesis of barbacic acid

A new approach for the synthesis of the active barbatic acid has been achieved in eight steps with 22.3% total yield by using commercially available methyl atratate as starting material. This synthesis provides access to multi-gram quantities of barbatic