120034-22-2

Upstream product

• 106-95-6 allyl bromide 
• 120034-16-4 4-hydroxy-7-chloro-2-<(4'-methoxyphenyl)methyl>-3-methylbenzofuran 
• 2632-13-5 2-Bromo-4'-methoxyacetophenone 
• 120034-13-1 4-hydroxy-7-chloro-5-tert-butyl-2-<(4'-methoxyphenyl)methyl>-3-methylbenzofuran 
• 120034-10-8 3-chloro-5-tert-butyl-2,6-dihydroxyacetophenone 

Downstream Products

• 120034-25-5 3-[7-Chloro-2-(4-methoxy-benzyl)-3-methyl-4-(1-methyl-1-trimethylsilanyl-ethoxy)-benzofuran-5-yl]-propionic acid 
• 120034-24-4 3-[7-Chloro-2-(4-methoxy-benzyl)-3-methyl-4-(1-methyl-1-trimethylsilanyl-ethoxy)-benzofuran-5-yl]-propan-1-ol 
• 120034-23-3 {1-[5-Allyl-7-chloro-2-(4-methoxy-benzyl)-3-methyl-benzofuran-4-yloxy]-1-methyl-ethyl}-trimethyl-silane 
• 120034-20-0 4-hydroxy-5-(carboxyethyl)-7-chloro-2-<(4'-methoxyphenyl)methyl>-3-methylbenzofuran 
• 120034-19-7 4-hydroxy-5-(hydroxypropyl)-7-chloro-2-<(4'-methoxyphenyl)methyl>-3-methylbenzofuran 
• 120034-18-6 5-allyl-4-hydroxy-7-chloro-2-<(4'-methoxyphenyl)methyl>-3-methylbenzofuran 

Relevant academic research and scientific papers

Benzofuran derivatives useful as inhibitors of mammalian leukotriene biosynthesis

Benzofuran derivatives, pharmaceutical compositions and methods of treatment are disclosed. These compounds are useful as inhibitors of mammalian leukotriene biosynthesis. As such, these compounds are useful therapeutic agents for treating allergic condit

Synthesis and Structure-Activity Relationships of a Novel Class of 5-Lipoxygenase Inhibitors. 2-(Phenylmethyl)-4-hydroxy-3,5-dialkylbenzofurans: The Development of L-656,224

The synthesis of a series of 2-(phenylmethyl)-4-hydroxy-3,5-dialkylbenzofurans and their inhibitory effects against leukotriene biosynthesis and 5-lipoxygenase activity in vitro are described.Many compounds of this series were found to be potent inhibitor