60555-93-3

Basic information

• Product Name: 6-BROMO-2,3-DIMETHOXYBENZOIC ACID
• Synonyms: Benzoic acid, 6-bromo-2,3-dimethoxy-
• CAS NO: 60555-93-3
• Molecular Formula: C₉H₉BrO₄
• Molecular Weight: 261.07
• Mol File: 60555-93-3.mol
• Article Data: 11

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 6-BROMO-2,3-DIMETHOXYBENZOIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 6-BROMO-2,3-DIMETHOXYBENZOIC ACID(60555-93-3)
• EPA Substance Registry System: 6-BROMO-2,3-DIMETHOXYBENZOIC ACID(60555-93-3)

Safety Data

• Hazardous Substances Data: 60555-93-3(Hazardous Substances Data)

Usage

General Description

6-Bromo-2,3-dimethoxybenzoic acid is a chemical compound with the molecular formula C9H9BrO4. It is a white to off-white crystalline powder that is commonly used as a building block in organic synthesis and pharmaceutical research. 6-BROMO-2,3-DIMETHOXYBENZOIC ACID is known for its ability to modify and enhance the properties of other chemical compounds, making it a valuable tool in drug development and medicinal chemistry. It is also used as a key intermediate in the synthesis of various bioactive compounds and pharmaceuticals. Additionally, 6-Bromo-2,3-dimethoxybenzoic acid has applications in the field of agrochemicals and materials science, and it is known for its diverse range of uses in chemical research and production.

Upstream product

• 53811-50-0 6-bromo-2,3-dimethoxybenzaldehyde 
• 77-48-5 1,3-dibromo-5,5-dimethylimidazolidine-2,4-dione 
• 1521-38-6 2,3-dimethoxybenzoic acid 
• 64482-27-5 2-bromo-5,6-dimethoxybenzoyl chloride 
• 83983-71-5 6-bromo-2,3-dihydroxybenzaldehyde 
• 20035-45-4 6-bromo-3-ethoxy-2-hydroxybenzaldehyde 
• 492-88-6 3-ethoxysalicylaldehyde 
• 7150-01-8 2-acetoxy-3-methoxybenzaldehyde 
• 20035-41-0 6-bromo-2-hydroxy-3-methoxybenzaldehyde 
• 5653-51-0 6-amino-2,3-dimethoxybenzoic acid 

Downstream Products

• 1521-38-6 2,3-dimethoxybenzoic acid 
• 59084-77-4 methyl 6-bromo-2,3-dimethoxybenzoate 
• 64482-29-7 2-(6'-bromo-2',3'-dimethoxybenzoyl)-1-methylene-6,7-methylenedioxy-1,2,3,4-tetrahydroisoquinoline 
• 64482-28-6 2-(6'-bromo-2',3'-dimethoxybenzoyl)-6,7-dimethoxy-1-methylene-1,2,3,4-tetrahydroisoquinoline 
• 187272-11-3 (7-Benzenesulfonyl-6-hydroxy-1,2,4,5,6,7-hexahydro-azocino[5,4-b]indol-3-yl)-(6-bromo-2,3-dimethoxy-phenyl)-methanone 
• 187272-12-4 7-Benzenesulfonyl-3-(6-bromo-2,3-dimethoxy-benzoyl)-1,2,3,4,5,7-hexahydro-azocino[5,4-b]indol-6-one 
• 157034-62-3 7-(6-Bromo-2,3-dimethoxy-benzoyl)-9-phenylsulfanyl-6,7,8,9-tetrahydro-5H-1,3-dioxa-7-aza-cycloocta[f]inden-10-one 
• 185245-95-8 N-(6-bromo-2,3-dimethoxybenzoyl)-6-hydroxy-8,9-methylenedioxy-1,2,3,4,5,6-hexahydro-3-benzazocine 
• 157034-61-2 N-(6-bromo-2,3-dimethoxybenzoyl)-8,9-methylenedioxy-6-oxo-1,2,3,4,5,6-hexahydro-3-benzazocine 
• 181634-60-6 6-bromo-2,3-dimethoxy-N-methyl-N-(6,7-methylenedioxynaphthalen-1-yl)benzamide 
• 181634-59-3 6-Bromo-2,3-dimethoxy-N-(6,7-methylenedioxy-1-naphthyl)benzamide 
• 28342-33-8 oxychelerythrine 
• 385390-29-4 N-(2-benzo[1,3]dioxol-5-yl-ethyl)-6-bromo-N-(2,2-dimethyl-4H-[1,3]dioxon-5-yl)-2,3-dimethoxy-benzamide 
• 385390-28-3 7-(6-bromo-2,3-dimethoxy-benzoyl)-6,7,8,9-tetrahydro-5H-1,3-dioxa-7-aza-cyclohepta[f]indene-6-carbaldehyde 

Relevant articles and documents

A short synthesis of lennoxamine via ynamides

Lennoxamine was synthesized in eight steps from 2,3-dimethoxybenzoic acid via an intermediate ynamide by using palladium-catalyzed Heck-Suzuki-Miyaura domino reactions.

Microwave-assisted domino hydroformylation/cyclization reactions: Scope and limitations

Hydroformylation of alkenes can be carried out in short time and with low syngas pressure under microwave (MW) dielectric heating. Alkenes, carrying O-, N-, or C-nucleophilic fragments, can be designed for domino reactions, mainly cyclocondensations. Ally

Structure-activity relationship studies of phenanthridine-based Bcl-X L inhibitors

Despite their structural similarities, the natural products chelerythrine (5) and sanguinarine (6) target different binding sites on the pro-survival Bcl-XL protein. This paper details the synthesis of phenanthridine-based analogues of the natu