5463-22-9

Usage

Uses

Used in Pharmaceutical Industry:
1,2-bis(4-hydroxy-3-methoxyphenyl)ethane-1,2-dione is used as a potential therapeutic agent for various diseases due to its antioxidant, anti-inflammatory, and anti-cancer properties.
Used in Nutraceutical Industry:
1,2-bis(4-hydroxy-3-methoxyphenyl)ethane-1,2-dione is used as a dietary supplement for its potential health benefits, including its antioxidant and anti-inflammatory properties.
Used in Cosmetic Industry:
1,2-bis(4-hydroxy-3-methoxyphenyl)ethane-1,2-dione is used as an ingredient in cosmetic products for its potential skin health benefits, including its antioxidant and anti-inflammatory properties.
Note: The uses listed above are based on the potential properties of 1,2-bis(4-hydroxy-3-methoxyphenyl)ethane-1,2-dione as mentioned in the provided materials. Further research is needed to fully understand its biological activities and potential applications in these industries.

Upstream product

• 4464-75-9 1,2-bis-(4-hydroxy-3-methoxyphenyl)ethane-1,2-diol 
• 4464-75-9 hydrovanilloin 
• 121-33-5 vanillin 

Downstream Products

• 5623-44-9 4,4’-dihydroxy-3,3’-dimethoxybenzophenone 
• 18256-53-6 4,4’-dihydroxy-3,3’-dimethoxybibenzyl 
• 4464-75-9 1,2-bis-(4-hydroxy-3-methoxyphenyl)ethane-1,2-diol 
• 61445-49-6 bis(3,4-dihydroxyphenyl)methanone 
• 5438-67-5 1,2-bis(4-hydroxy-3-methoxyphenyl)-1-ethanone 
• 5463-23-0 4,4'-Dihydroxy-3,3'-dimethoxy-benzoin 
• 54704-87-9 4,4'-Diacetoxy-3,3'-dimethoxy-benzil 
• 96970-14-8 4,4'-Bis-benzyloxy-3,3'-dimethoxy-benzil 
• 875245-90-2 4-Allyloxy-4'-hydroxy-3,3'-dimethoxy-benzil 
• 7508-46-5 4,4'-Bis-allyloxy-3,3'-dimethoxy-benzil 
• 5963-51-9 1,2-bis(3,4-dimethoxyphenyl)ethane 
• 7329-69-3 (E)-3,3'-dimethoxy-4,4'-dihydroxystilbene 
• 109219-48-9 3,4,3',4'-tetrahydroxybenzoin 
• 100622-09-1 3,4,3',4'-tetrahydroxydesoxybenzoin 

Relevant academic research and scientific papers

Quinone Dehydrogenation. Oxidation of Benzylic Alcohols with 2,3-Dichloro-5,6-dicyanobenzoquinone

2,3-Dichloro-5,6-dicyanobenzoquinone (DDQ) reacts with primary and secondary aryl-substituted alcohols under mild conditions in dioxane solution to give the corresponding carbonyl compounds in high yields.In contrast to other oxidants, DDQ can be applied advantageously for the oxidation of hydroxyaryl-substituted alcohols.A mechanism involving participation of the phenolic hydroxyl group in the dehydrogenation reaction is discussed.Oxidations of hydroxyaryl-substituted alcohols by DDQ in methanolsolution resulting in the formation of benzoquinones by loss of the hydroxyaryl side chain are interpreted in terms of phenol oxidation.An example of a pyridine-catalyzed Smiles rearrangement of an o-hydroxy-substituted diphenyl ether is reported.