72935-22-9

Upstream product

• 34874-90-3 methyl haematommate 
• 100-39-0 benzyl bromide 
• 3187-58-4 methyl orsellinate 
• 126717-83-7 methyl 3-formyl-2,4-dimethoxy-6-methylbenzoate 

Downstream Products

• 72935-23-0 methyl 2,4-dibenzyloxy-3-hydroxy-6-methylbenzoate 
• 158183-41-6 6-benzyl 2-methyl 3,9-dihydroxy-4-methoxy-1,7-dimethydibenzofuran-2,6-dicarboxylate 
• 158183-40-5 benzyl 4-hydroxy-2-(3'-hydroxy-2'-methoxy-4'-methoxycarbonyl-5'-methylphenoxy)-6-methylbenzoate 
• 158183-37-0 methyl 4-(4'-benzyloxy-2'-hydroxy-6'-methylbenzyloxy)-2-hydroxy-3-methoxy-6-methylbenzoate 
• 158183-38-1 4-benzyloxy-2-(3'-hydroxy-2'-methoxy-4'-methoxycarbonyl-5'-methylphenoxy)-6-methylbenzoic acid 
• 158183-35-8 methyl 2,4-dibenzyloxy-3-methoxy-6-methylbenzoate 
• 158183-39-2 4-hydroxy-2-(3'-hydroxy-2'-methoxy-4'-methoxycarbonyl-5'-methylphenoxy)-6-methylbenzoic acid 
• 158183-36-9 methyl 2,4-dihydroxy-3-methoxy-6-methylbenzoate 

Relevant academic research and scientific papers

The Structure and Synthesis of 4-Oxypannaric Acid 2-Methyl Ester, a Dibenzofuran from the Lichen Leproloma diffusum

The structure of the major dibenzofuran present in the lichen Leproloma diffusum has been shown to be that of 4-oxypannaric acid 2-methyl ester (2-methyl hydrogen 3,4,9-trihydroxy-1,7-dimethyldibenzofuran-2,6-dicarboxylate) (2).The structure of (2) was co

Synthese du virensate de methyle

The synthesis of methyl virensate (=methyl 4-formyl-3,8-dihydroxy-1,6,9-trimethyl-11-oxo-11H-dibenzodioxepin-7-carboxylate; 18) by the condensation of the substituted β-orcinol and orcinol units 9 and 10 followed by formylation and demethylation