120694-92-0

Upstream product

• 120694-96-4 6-(3-(2-hydroxymethylphenyl)-trans-prop-2-enyl)-5-hydroxy-2,3-dihydrobenzofuran 
• 64-17-5 ethanol 
• 6630-33-7 ortho-bromobenzaldehyde 
• 124854-97-3 6-<3-(2-Cyanophenyl)-2-propenyl>-2,3-dihydro-5-hydroxybenzofuran 
• 124854-98-4 2-<3-(2,3-dihydro-5-hydroxy-6-benzofuranyl)-1-propenyl>benzaldehyde 
• 124854-96-2 6-<3-(2-Bromophenyl)-2-propenyl>-2,3-dihydro-5-hydroxybenzofuran 
• 124854-94-0 (E)-3-(2-bromophenyl)-2-propen-1-ol 
• 124854-95-1 (E)-1-bromo-2-(3-bromoprop-1-en-1-yl)benzene 
• 91047-77-7 ethyl (2E)-3-(2-bromophenyl)prop-2-enoate 
• 40492-52-2 2,3-dihydrobenzofuran-5-ol 

Relevant academic research and scientific papers

Antioxidant-Based Inhibitors of Leukotriene Biosynthesis. The Discovery of 6--1-propen-3-yl>-2,3-dihydro-5-benzofuranol, a Potent Topical Antiinflammatory Agent

The leukotrienes, metabolites of arachidonic acid produced through the action of the enzyme 5-lipoxygenase, are important mediators of immediate hypersensitivity and inflammation.Among the variety of diseases in which the leukotrienes may play a symptomat

Phenylpropyl-2,3-dihydrobenzofurans useful as anti-inflammatory agents

Phenylalkyl-2,3-dihydrobenzofurans and analogs were prepared by (1) nucleophilic substitution involving an appropriately substituted 2,3-dihydrobenzofuranol (or 2,3-dihydrobenzopyranol) and a cinnamylhalide followed by reduction; or (2) by Wittig reaction