60241-74-9

Usage

Uses

Used in Pharmaceutical Industry:
2,3,6-Trimethoxybenzoic acid is used as a key intermediate in the synthesis of various pharmaceuticals for its potential anti-inflammatory and analgesic properties. It aids in the development of new therapeutic agents that can provide relief from inflammation and pain.
Used in Organic Chemical Reactions:
As an intermediate in organic chemical reactions, 2,3,6-Trimethoxybenzoic acid plays a crucial role in the production of various organic compounds. Its unique chemical structure allows it to participate in a wide range of reactions, contributing to the synthesis of diverse chemical products.
Used in Antioxidant Applications:
2,3,6-Trimethoxybenzoic acid is used as an antioxidant in various applications, including pharmaceuticals and cosmetics. Its antioxidant properties help protect cells from damage caused by free radicals, thereby promoting overall health and well-being.
Used in Antimicrobial Applications:
Due to its antimicrobial properties, 2,3,6-Trimethoxybenzoic acid is used in the development of antimicrobial agents. It can be employed in the formulation of products that help combat bacterial and fungal infections, contributing to improved hygiene and health.

InChI:InChI=1/C10H12O5/c1-13-6-4-5-7(14-2)9(15-3)8(6)10(11)12/h4-5H,1-3H3,(H,11,12)

Upstream product

• 135-77-3 1,2,4-trimethoxy-benzene 
• 15719-64-9 methylammonium carbonate 
• 72517-26-1 2,3-dimethoxy-6-nitrobenzoic acid 
• 60241-75-0 methyl 2,3,6-trimethoxybenzoate 
• 5653-53-2 6-hydroxy-2,3-dimethoxy-benzoic acid 
• 77-78-1 dimethyl sulfate 
• 16534-78-4 2,3,6-trihydroxybenzoic acid 
• 25576-97-0 2,3,6-trimethoxytoluene 

Downstream Products

• 60241-75-0 methyl 2,3,6-trimethoxybenzoate 
• 101460-33-7 3-Bromo-2,5,6-trimethoxy-benzoyl chloride 
• 98601-22-0 N-((S)-1-Ethyl-pyrrolidin-2-ylmethyl)-2-hydroxy-3,6-dimethoxy-benzamide 
• 101460-64-4 (S)-(-)-N-[(1-Ethyl-2-pyrrolidinyl)methyl]-2-hydroxy-5,6-dimethoxybenzamide 
• 101460-26-8 N-((S)-1-Ethyl-pyrrolidin-2-ylmethyl)-2,3,6-trimethoxy-benzamide 
• 101460-42-8 3-Chloro-N-((S)-1-ethyl-pyrrolidin-2-ylmethyl)-6-hydroxy-2,5-dimethoxy-benzamide 
• 101460-23-5 (S)-(-)-N-[(1-ethyl-2-pyrrolidinyl)methyl]-3-chloro-2,5,6-trimethoxybenzamide 
• 101460-52-0 N-((S)-1-Allyl-pyrrolidin-2-ylmethyl)-3-bromo-6-hydroxy-2,5-dimethoxy-benzamide 
• 101460-53-1 (S)-N-<(1-allyl-2-pyrrolidinyl)methyl>-3-bromo-2,5,6-trimethoxybenzamide 
• 125198-32-5 (S)-3-bromo-N-(2-pyrrolidinylmethyl)-2,5,6-trimethoxybenzamide 
• 101460-41-7 (S)-(-)-N-[(1-ethyl-2-pyrrolidinyl)methyl]-3-chloro-2-hydroxy-5,6-dimethoxybenzamide 
• 101460-66-6 FLB 463 
• 125198-24-5 3-Bromo-N-((R)-1-ethyl-pyrrolidin-2-ylmethyl)-2-hydroxy-5,6-dimethoxy-benzamide 
• 102727-69-5 3-Bromo-N-((S)-1-ethyl-pyrrolidin-2-ylmethyl)-6-hydroxy-2,5-dimethoxy-benzamide 

Relevant academic research and scientific papers

Method for preparing 1,3,5,8-tetrahydroxy xanthone and 1,3,7,8-tetrahydroxy xanthone

The invention discloses a method for preparing 1,3,5,8-tetrahydroxy xanthone and 1,3,7,8-tetrahydroxy xanthone. The method comprises the following steps: by taking 1,2,4-trimetoxybenzene as an initialraw material, and adding n-butyllithium and a chloro-ca

Structure of leiocarposide

Leiocarpic acid (3,6-dihydroxy-2-methoxy-benzoic acid), a new benzoic acid derivative was obtained from leiocarposide, a phenolic glycoside from Solidago virgaurea var. leiocarpa (Benth) A.Gray and Solidago virgaurea L.In the revised structure, leiocarpos