26880-96-6

Upstream product

• 58600-95-6 4-methylphenyl 4-methoxybenzoate 
• 25045-35-6 2-methoxy-5-methylbenzoyl chloride 
• 100-66-3 methoxybenzene 
• 613-84-3 2-hydroxy-5-methylbenzaldehyde 
• 46441-20-7 Phenyl-(4-methoxy-phenyl)-iodonium 
• 104-93-8 p-methylanizole 
• 100-07-2 4-methoxy-benzoyl chloride 

Downstream Products

• 677707-47-0 ethyl [2-(4-methoxybenzoyl)-4-methylphenoxy]acetate 
• 1630042-89-5 2 [2 (4 methoxybenzoyl) 4 methylphenoxy]methyl-1,3,4 oxadiazole 
• 1578261-45-6 N'-{2-[2-(4-methoxybenzoyl)-4-methylphenoxy]acetyl}coumarin-3-carbohydrazide 
• 1578261-59-2 ethyl (N'-{2-[2-(4-methoxybenzoyl)-4-methylphenoxy]acetyl}hydrazinocarbonyl)acetate 
• 677707-55-0 [2-(5-amino-[1,3,4]oxadiazol-2-ylmethoxy)-5-methyl-phenyl]-(4-methoxy-phenyl)-methanone 
• 677707-51-6 2-[2-(4-methoxybenzoyl)-4-methylphenoxy]acetohydrazide 
• 871037-29-5 [2-(4-amino-5-thioxo-4,5-dihydro-1H-[1,2,4]triazol-3-ylmethoxy)-5-methyl-phenyl]-(4-methoxy-phenyl)-methanone 
• 871037-24-0 (4-methoxy-phenyl)-[5-methyl-2-(5-thioxo-4,5-dihydro-[1,3,4]oxadiazol-2-ylmethoxy)-phenyl]-methanone 
• 725744-71-8 [2-(4-methoxy-benzoyl)-4-methyl-phenoxy]-acetic acid 
• 54118-71-7 2,4'-dimethoxy-5-methyl-benzophenone 

Relevant academic research and scientific papers

Hypervalent iodine in synthesis XXXIV: Palladium-catalyzed coupling reaction of o-hydroxyarylaldehydes with hypervalent iodonium salts via cleavage of the aldehyde C-H bond

A novel way of preparation for o-hydroxyarylketones with mild conditions and good yields by palladium-catalyzed coupling reaction of o- hydroxyarylaldehydes with hypervalent iodonium salts via the cleavage of the aldehyde C-H bond has been reported.

Synthesis and anti-inflammatory activity of benzophenone analogues

A series of substituted benzophenone analogues has been synthesized and evaluated as orally active anti-inflammatory agents with reduced side effects. The anti-inflammatory and ulcerogenic activities of the compounds were compared with naproxen, indometha