61637-60-3

Usage

Uses

Used in Pharmaceutical Industry:
3,5-Dimethoxysalicylic acid is used as a building block for the synthesis of various drugs, particularly anti-inflammatory and analgesic agents, due to its versatile chemical structure and properties.
Used in Antioxidant Applications:
3,5-Dimethoxysalicylic acid is used as an antioxidant agent, potentially protecting cells from oxidative damage and contributing to overall health and wellness.
Used in Anti-Cancer Applications:
3,5-Dimethoxysalicylic acid is used as a potential anti-cancer agent, with ongoing research exploring its therapeutic applications in the prevention and treatment of cancer.

InChI:InChI=1/C9H10O5/c1-13-5-3-6(9(11)12)8(10)7(4-5)14-2/h3-4,10H,1-2H3,(H,11,12)

Upstream product

• 36873-96-8 2,3,5-trimethoxybenzoic acid 
• 33580-60-8 2,3,5-trihydroxybenzoic acid 
• 77-78-1 dimethyl sulfate 
• 17275-86-4 2-bromo-3,5-dimethoxybenzoic acid 
• 99-10-5 3,5-Dihydroxybenzoic acid 
• 1132-21-4 3,5-dimethoxybenzoic acid 
• 19491-18-0 methyl 2-bromo-3,5-dimethoxybenzoate 
• 2150-37-0 methyl 3,5-dimethoxybenzoate 

Downstream Products

• 946408-35-1 3,5-dimethoxysalicylic alcohol 
• 93092-12-7 2'-hydroxy-3',5,5',6,7-pentamethoxyflavone 
• 93092-11-6 2'-benzyloxy-3',5,5',6,7-pentamethoxyflavone 
• 93092-10-5 1-(2-Benzyloxy-3,5-dimethoxy-phenyl)-3-(6-hydroxy-2,3,4-trimethoxy-phenyl)-propane-1,3-dione 
• 93092-09-2 2-(2'-benzyloxy-3',5'-dimethoxybenzoyloxy)-4,5,6-trimethoxyacetophenone 
• 93092-13-8 2',5-dihydroxy-3',5',6,7-tetramethoxyflavone 
• 946408-42-0 C₂₀H₂₄O₅ 
• 946408-41-9 C₂₂H₂₀O₅ 
• 946408-40-8 C₁₈H₂₀O₄ 
• 946408-38-4 3,5-dimethoxy-α,α-dimethylsalicylic alcohol 
• 99187-06-1 2-hydroxy-3,5-dimethoxy-benzoic acid methyl ester 

Relevant academic research and scientific papers

Application of the excited state meta effect in photolabile protecting group design

A novel photolabile protecting group for carbonyl compounds has been developed, based on the excited state meta effect.

Synthetic Studies on the Flavone Derivatives. XII. Synthesis of 2',3',5'- and 3',4',5'-Trioxygenated Flavones

Two unusual flavones, 5,5'-dihydroxy-2',3',6,7-tetramethoxyflavone (1) from Gardenia cramerii and 4',5-dihydroxy-3',5',6,7-tetramethoxyflavone (6) from Artemisia mesatlantia, and their position isomers were synthesized to investigate the structural correlation in terms of spectral data.The structure of the flavone from G. cramerii is discussed.Keywords: 5,5'-dihydroxy-2',3',6,7-tetramethoxyflavone; 2',5-dihydroxy-3',5',6,7-tetramethoxyflavone; 5-hydroxy-2',3',5',6,7-pentamethoxyflavone; 3',5-dihydroxy-4',5',6,7-tetramethoxyflavone; 4',5-dihydroxy-3',5',6,7-tetramethoxyflavone; 5-hydroxy-3',4',5',6,7-pentamethoxyflavone.