41252-35-1

Upstream product

• 6257-22-3 2,6-di-t-butyl-4-(4-methoxyphenyl)phenol 
• 104-92-7 1-bromo-4-methoxy-benzene 
• 719-22-2 2,6-Di-tert-butyl-1,4-benzoquinone 

Downstream Products

• 69892-33-7 2,6-Di-tert-butyl-4-hydroperoxy-4-(4-methoxy-phenyl)-cyclohexa-2,5-dienone 
• 58459-54-4 2,6-Di-tert-butyl-4-(4-methoxy-phenyl)-1-p-tolyl-cyclohexa-2,5-diene-1,4-diol 
• 74233-22-0 2,6-Di-tert-butyl-4-methoxy-4-(4-methoxy-phenyl)-cyclohexa-2,5-dienone 

Relevant academic research and scientific papers

Field control of regioselectivity in CoIII(salpr)(OH) promoted oxygenation of 4-aryl-2,6-di-terf-butylphenols

In the CoIII(salpr)(OH) catalyzed oxygenation of 4-aryl-2,6-di-tert-butylphenols, the position of dioxygen incorporation is completely controlled by the nature of solvent; dioxygen incorporation occurs only at ortho position in an uncoordinativ

Anti-inflammatory method

Compounds in which 2,6-di(t-butyl)phenol is substituted in the 4 position by an optionally substituted phenyl group having valuable pharmacological activity as anti-inflammatory agents.