60824-63-7

Upstream product

• 93-51-6 2-Methoxy-4-methylphenol 
• 123752-64-7 6<(dimethylamino)methyl>-2-methoxy-4-methylphenol 
• 1125-67-3 3-methoxy-5-methylbenzene-1,2-diol 

Downstream Products

• 6638-05-7 2,6-dimethoxy-4-methylphenol 
• 60824-64-8 4-hydroxy-3,5-dimethoxybenzyl methyl ether 
• 91971-33-4 2-Acetonyl-3-methoxy-5-methyl-o-benzochinol 
• 1256550-28-3 6,6-difluoro-5-methoxy-3-methylcyclohexa-2,4-dienone 
• 447462-92-2 2-fluoro-3-methoxy-5-methylphenol 

Relevant academic research and scientific papers

Nucleophilic deoxyfluorination of catechols

Nucleophilic deoxyfluorinaiton of one of the two hydroxyl groups of catechols has been developed via the Umpolung concept. This method was successively applied to naturally occurring catechols, such as catechins and dopamine, to produce novel fluorinated

Oxidative Degradation of 6-Hydroxy-1,2,3,4-tetrahydroisoquinolines and 7-Hydroxy-2-benzazepines. A Novel Route to Heterocyclic Quinones

A novel route toward 4,5-indolequinones and 5,8-quinolinequinones, based on the Fremy's salt promoted oxidative degradation of 6-hydroxy-1,2,3,4-tetrahydroisoquinolines and 7-hydroxy-2-benzazepines, is described.