33974-40-2

Upstream product

• 67-56-1 methanol 
• 16373-02-7 2,4-di-tert-butyl-6-hydroxymethylphenol 
• 15515-54-5 2-methoxy-4,6-di-tert-butylphenol 

Downstream Products

• 100699-37-4 2,4-di-t-butyl-4,6-dimethoxycyclohexa-2,5-dienone 

Relevant academic research and scientific papers

Photooxygenation of masked o-benzoquinones: An efficient entry into highly functionalized cyclopentenones from 2-methoxyphenols

(Chemical Equation Presented) MOB tactics: A novel oxidation of masked o-benzoquinones (MOBs) 1 occurs by singlet-oxygen-triggered ring contraction to form cyclopentenone derivatives 2 and by [4+2] cycloaddition to give endoperoxides 3. The competing path

1,3-Methoxy rearrangement of masked o-benzoquinones: A novel synthesis of p-quinol ethers

(Chemical Equation Presented) p-Quinol ethers are valuable synthons in synthetic organic chemistry. MOBs 1a-1l can be converted to p-quinol ethers 2a-2i in a highly efficient manner via 1,3-methoxy migration catalyzed by Lewis acids. The migration was fou