412344-56-0

Upstream product

• 55171-62-5 2-bromo-4,5-methylenedioxybenzoyl chloride 
• 60546-62-5 6-bromopiperonylic acid 
• 1588511-69-6 N-methoxy-N-methyl-6-vinylbenzo[d][1,3]dioxole-5-carboxamide 
• 133095-91-7 3,4,5-trimethoxyphenylmagnesium bromide 
• 15930-53-7 6-bromo-3,4-methylenedioxybenzaldehyde 
• 4521-61-3 3,4,5-Trimethoxybenzoyl chloride 
• 1484-85-1 3,4-methylenedioxyphenylethylamine 
• 5422-05-9 3,4,5-trimethoxy-benzoic acid homopiperonylamide 
• 412344-59-3 5-(3,4,5-trimethoxy-phenyl)-7,8-dihydro-[1,3]dioxolo[4,5-g]isoquinoline 
• 77-78-1 dimethyl sulfate 

Downstream Products

• 1588511-84-5 5-methyl-8-(3,4,5-trimethoxyphenyl)-[1,3]dioxolo[4,5-g]phthalazines 
• 938154-92-8 1-[6-(3,4,5-trimethoxybenzoyl)benzo[d][1,3]dioxol-5-yl]ethanone 
• 7470-99-7 2-(3,4,5-Trimethoxybenzoyl)-4,5-(methylenedioxy)benzoic Acid 
• 5423-32-5 2'-formyl-4',5'-methylenedioxy-3,4,5-trimethoxybenzophenone 

Relevant academic research and scientific papers

Iodine-promoted oxidative conversion of o-vinyl diaryl ketones into o-acetyl diaryl ketones, synthesis of 1-methyl-4-arylphthalazines as analogues of podophyllotoxin

A new method is described for the metal-free oxidation of o-vinyl diaryl ketones in the presence of molecular iodine or N-iodosuccinimide to give o-acetyl diaryl ketones. This transformation involves the initial formation of an iodohydrin, and the o-carbo

Iodine-promoted oxidative conversion of o-vinyl diaryl ketones into o-acetyl diaryl ketones, synthesis of 1-methyl-4-arylphthalazines as analogues of podophyllotoxin

A new method is described for the metal-free oxidation of o-vinyl diaryl ketones in the presence of molecular iodine or N-iodosuccinimide to give o-acetyl diaryl ketones. This transformation involves the initial formation of an iodohydrin, and the o-carbo