3465-69-8

Usage

Uses

Used in Pharmaceutical and Medicinal Applications:
1(3H)-Isobenzofuranone, 5,7-dimethoxyis used as a pharmaceutical and medicinal compound for its antioxidant, anti-inflammatory, and neuroprotective effects. It is being researched for its potential as a treatment for various diseases and conditions, making it a subject of interest in the fields of pharmacology and drug development.
Used in Food Industry:
1(3H)-Isobenzofuranone, 5,7-dimethoxyis used as a flavoring agent in the food industry, contributing to the enhancement of taste and aroma in various products.
Used in Cosmetics Industry:
1(3H)-Isobenzofuranone, 5,7-dimethoxyis used as a fragrance ingredient in the cosmetics industry, providing a pleasant scent to various cosmetic products.

Upstream product

• 57061-31-1 3-benzenesulfinyl-5H-furan-2-one 
• 90857-62-8 Brassard's diene 
• 124-38-9 carbon dioxide 
• 74726-76-4 2-bromo-3,5-dimethoxybenzyl alcohol 
• 1132-21-4 3,5-dimethoxybenzoic acid 
• 705-76-0 3,5-dimethoxybenzyl alcohol 
• 13433-00-6 diethyl aminomalonate hydrochloride 
• 303044-37-3 2-(chloromethyl)-4,6-dimethoxy-benzoic acid 
• 166322-67-4 2-(chloromethyl)-4,6-dimethoxy-benzaldehyde 
• 124200-75-5 1,3-dihydro-5,7-dimethoxy-6-<(trifluoromethanesulfonyl)oxy>isobenzofuran-1-one 

Downstream Products

• 24953-77-3 7-hydroxy-5-methoxyisobenzofuran-1(3H)-one 
• 206130-70-3 3-(α-hydroxy-4-benzyloxy-3-methoxybenzyl)-5,7-dimethoxyphthalide 
• 206130-69-0 3-(α-hydroxy-3,4-dimethoxybenzyl)-5,7-dimethoxyphthalide 
• 107584-58-7 3-(3,4-dimethoxybenzyl)-7-hydroxy-5-methoxyphthalide 
• 206130-75-8 (Z)-3-(3,4-dimethoxybenzylidene)-7-hydroxy-5-methoxyphthalide 
• 206130-72-5 (Z)-3-(3,4-dimethoxybenzylidene)-5,7-dimethoxyisobenzofuran-1(3H)-one 
• 206130-73-6 (Z)-3-(4-benzyloxy-3-methoxybenzylidene)-5,7-dimethoxyphthalide 
• 70719-39-0 2,4-Dimethoxy-6-phenylsulfanylmethyl-benzoic acid 
• 1224601-66-4 3-[13-(tert-butyldiphenylsilanyloxy)-10-oxotetradecyl]-5,7-dimethoxy-3H-isobenzofuran-1-one 
• 17846-89-8 2-formyl-4,6-dimethoxy-benzoic acid 
• 17846-90-1 methyl 2-formyl-4,6-dimethoxybenzoate 
• 6803-02-7 6-methoxymellein 
• 24280-93-1 mycophenolic acid 
• 37715-47-2 5,7-Dimethoxy-4-methylisobenzofuran-1(3H)-one 

Relevant academic research and scientific papers

Studies toward the synthesis of caramboxin analogues

Intrigued by the recent discovery of caramboxin by Brazilian researchers, we present the results from our studies toward the racemic synthesis of caramboxin analogs through the ortho-carboxylation of 3,5-dimethoxy benzyl derivatives. Three different approaches were tested, and the route involving a Vilsmeier-Haack formylation followed by a Lindgren oxidation provide a potential intermediate for the synthesis of several caramboxin analogs.

Deoxygenation of Highly Hindered Phenols

Highly hindered phenolic compounds can be efficiently deoxygenated by reduction of the corresponding triflates under homogeneous or heterogeneous (Pd/C) conditions.Reductive deoxygenation under homogeneous conditions has been shown to occur both in the presence of acid (HCOOH, CH3COOH, (CH3)3CCOOH, PhCH2COOH) or in its absence.The concomitant formation of dibutylformamide apparently derives from aminolysis of DMF by dibutylamine, the Pd(0)-catalyzed hydrolysis product of tributylamine.Deuteration experiments suggest that several hydrogen (or deuterium) sources operate in the hydrogenolysis processes studied.