1292688-03-9

Upstream product

• 1292688-12-0 methyl 3-(tert-butyldimethylsilyloxy)-2,6-dimethylbenzoate 
• 131236-69-6 methyl 2,6-dimethyl-3-hydroxybenzene-1-carboxylate 
• 18162-48-6 tert-butyldimethylsilyl chloride 
• 1260656-39-0 methyl 2,6-dimethyl-3-nitrobenzoate 
• 6307-70-6 2,6-dimethyl-3-nitrobenzoic acid 
• 269072-16-4 3-amino-2,6-dimethyl-benzoic acid methyl ester 
• 632-46-2 2,6-dimethylbenzoic acid 

Downstream Products

• 1357476-72-2 C₂₆H₃₈O₄Si 
• 1357476-73-3 3-[hydroxy(3-isopropenyl-4,5-dimethoxyphenyl)methyl]-2,4-dimethylphenol 
• 1357476-75-5 3-[hydroxy(3-isopropyl-4,5-dimethoxyphenyl)methyl]-2,4-dimethylphenol 
• 1357476-76-6 [3-(acetoxy)-2,6-dimethylphenyl](3-isopropyl-4,5-dimethoxyphenyl)methyl acetate 
• 1357476-77-7 3-[(acetoxy)-(2-bromo-3-isopropyl-4,5-dimethoxyphenyl)methyl]-2,4-dimethylphenyl acetate 
• 1357476-78-8 (2-bromo-3-isopropyl-4,5-dimethoxyphenyl)(3-hydroxy-2,6-dimethylphenyl)methyl acetate 
• 1357476-80-2 3-[(2-bromo-3-isopropyl-4,5-dimethoxyphenyl)(hydroxy)methyl]-2,4-dimethylphenol 
• 1357476-81-3 3-[(2-bromo-3-isopropyl-4,5-dimethoxyphenyl)(hydroxy)methyl]-2,4-dimethyl-4-(2,2,2-trifluoroethoxy)cyclohexa-2,5-dien-1-one 
• 1357476-82-4 C₂₇H₄₂O₅Si 
• 1357476-83-5 3-[hydroxy(3-isopropyl-2,4,5-trimethoxyphenyl)methyl]-2,4-dimethylphenol 
• 1357476-84-6 C₂₃H₂₉F₃O₆ 
• 1357476-85-7 C₂₇H₄₀O₅Si 
• 1357476-86-8 C₂₁H₂₆O₅ 
• 1357476-87-9 3-(3-isopropyl-2,4,5-trimethoxybenzoyl)-2,4-dimethyl-4-(2,2,2-trifluoroethoxy)cyclohexa-2,5-dien-1-one 

Relevant academic research and scientific papers

3-SUBSTITUTED COMPOUNDS FOR REDUCING URIC ACID

Uric acid in mammalian subjects is reduced and excretion of uric acid is increased by administering a compound of Formula 1. The uric acid-lowering effects of the compounds of this invention are used to treat or prevent a variety of conditions including g

Synthetic approach to 4a-methyltetrahydrofluorene-type diterpenoids via an aromatic oxidation of phenol derivatives

An intramolecular aromatic oxidation of a phenolic compound with a hypervalent iodine reagent afforded the coupling product, in which the coupling took place at the para-position of the methoxy goup of the starting material instead of the desired para-pos