29976-81-6

Upstream product

• 1450-72-2 5-methyl-2-hydroxyacetophenone 
• 100-07-2 4-methoxy-benzoyl chloride 
• 100-09-4 4-methoxybenzoic acid 

Downstream Products

• 35947-90-1 3-bromo-4'-methoxy-6-methylflavone 
• 52752-69-9 2-bromo-1-(2-hydroxy-5-methyl-phenyl)-3-(4-methoxy-phenyl)-propane-1,3-dione 
• 80649-90-7 3-(4-Methoxy-phenyl)-7-methyl-1-phenyl-1H-benzo[4,5]furo[3,2-c]pyrazole 
• 36695-31-5 (3-hydroxy-5-methyl-benzofuran-2-yl)-(4-methoxy-phenyl)-methanone 
• 65840-98-4 3-(2-hydroxy-5-methylphenyl)-5-(4-methoxyphenyl)pyrazole 
• 37689-62-6 2-[5-(4-methoxy-phenyl)-1-phenyl-1H-pyrazol-3-yl]-4-methyl-phenol 
• 136764-53-9 1a,7a-Dihydro-5-methyl-1a-(4-methoxyphenyl)-7H-oxireno<1>benzopyran-7-one 
• 6971-17-1 3-hydroxy-2-(4-methoxy-phenyl)-6-methyl-chromen-4-one 
• 29976-77-0 6-methyl-4'-methoxyflavone 
• 112753-49-8 3-(α-hydroxyamino-4-methylstyryl)-5-methylbenzisoxazole 
• 29976-91-8 3-(2-hydroxy-5-methylphenyl)-5-(4-methoxyphenyl)isoxazole 
• 80649-84-9 4-Methoxy-benzoic acid 2-(2-iodo-acetyl)-4-methyl-phenyl ester 
• 29976-84-9 1-(2-hydroxy-5-methylphenyl)-3-(4-methoxyphenyl)propane-1,3-dione 

Relevant academic research and scientific papers

Epoxidation of Flavones by Dimethyldioxirane

The synthesis of epoxides 2 by epoxidation of flavones 1 with isolated dimethyldioxirane (as acetone solution) at subambient temperatures is reported.These labile epoxides were isolated and completely characterized by UV, IR, 1H and 13C NMR, MS, and C,H analyses.Warming to room temperature led to rearrangement to afford quantitatively the 3-hydroxyflavones 3b,h,i,n.Treatment of the epoxides 2b,f with methanol led to the 3-hydroxy-2-methoxyflavanones 4b,f, as a mixture of cis and trans isomers.