73219-89-3

Basic information

• Product Name: 3-BROMO-2,6-DIMETHOXYBENZOIC ACID
• Synonyms: BUTTPARK 48\04-87;3-BROMO-2,6-DIMETHOXYBENZOIC ACID;3-Bromo-2,6-dimethoxybenzoic acid , 97+%
• CAS NO: 73219-89-3
• Molecular Formula: C₉H₉BrO₄
• Molecular Weight: 261.07
• Product Categories: Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts
• Mol File: 73219-89-3.mol
• Article Data: 6

Chemical Properties

• Melting Point: 146 °C
• Boiling Point: 359.8°C at 760 mmHg
• Flash Point: 171.4°C
• Appearance: /
• Density: 1.571g/cm³
• Vapor Pressure: 8.38E-06mmHg at 25°C
• Refractive Index: 1.566
• Storage Temp.: -20°C Freezer, Under inert atmosphere
• Solubility: Chloroform (Slightly), DMSO (Slightly), Ethyl Acetate (Slightly)
• PKA: 3.59±0.10(Predicted)
• CAS DataBase Reference: 3-BROMO-2,6-DIMETHOXYBENZOIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 3-BROMO-2,6-DIMETHOXYBENZOIC ACID(73219-89-3)
• EPA Substance Registry System: 3-BROMO-2,6-DIMETHOXYBENZOIC ACID(73219-89-3)

Safety Data

• Statements: 36/37/38
• Safety Statements: 26-37
• Hazardous Substances Data: 73219-89-3(Hazardous Substances Data)

Usage

General Description

3-Bromo-2,6-dimethoxybenzoic acid is a chemical compound with the molecular formula C9H9BrO4. It is a white solid that is insoluble in water but soluble in organic solvents. 3-BROMO-2,6-DIMETHOXYBENZOIC ACID is commonly used in organic synthesis as a building block to create new chemical compounds with specific properties. It is also used in research and development for its potential applications in the pharmaceutical and agrochemical industries. Additionally, it has been studied for its potential biological activities and effects, such as antifungal and antimicrobial properties.

InChI:InChI=1/C9H9BrO4/c1-13-6-4-3-5(10)8(14-2)7(6)9(11)12/h3-4H,1-2H3,(H,11,12)

Upstream product

• 1466-76-8 2-6-dimethoxybenzoic acid 
• 65977-12-0 3-Brom-2,6-dimethoxy-benzoesaeure-methylester 

Downstream Products

• 586392-15-6 3-bromo-2,6-dimethoxybenzyl alcohol 
• 73219-94-0 N-Ethyl-2-(3-bromo-2,6-dimethoxybenzamidomethyl)pyrrolidine hydrochloride 
• 1323988-61-9 (1S)-1,5-anhydro-2-deoxy-1-(3-bromo-2,6-dimethoxyphenyl)-3,4,6-tris-O-acetyl-D-erythro-hex-2-enitol 
• 1323988-65-3 (2R,3S,6S)-2-(acetoxymethyl)-6-(3-bromo-2,6-dimethoxyphenyl)-3,6-dihydro-2H-pyran-3,4-diyl diacetate 
• 1356488-33-9 C₁₂H₁₀BrClO₂S 
• 73219-92-8 3-bromo-5-chloro-2,6-dimethoxybenzoic acid 
• 84225-91-2 5-bromo-2,6-dimethoxybenzoic acid chloride 

Relevant articles and documents

New anthracene derivatives from Coussarea macrophylla

Five new naturally occurring anthracene derivatives, 1,4,10-trimethoxyanthracene-2-carbaldehyde (1), (1,4,10-trimethoxy-2-anthracen-2-yl)methanol (2), 1,4,8,10-tetramethoxyanthracene-2-carbaldehyde (3), 1,4,10-trimethoxyanthracene-2-carboxylic acid (4), a

N-bromosuccinimide/dibromodimethylhydantoin in aqueous base: A practical method for the bromination of activated benzoic acids

A new bromination method employing NBS or dibromodimethylhydantoin in aqueous base is described for the synthesis of 3-bromo-2,6-dimethoxybenzoic acid (1) and other monobrominated alkoxybenzoic acids.

Potential Neuroleptic Agents. 2,6-Dialkoxybenzamide Derivatives with Potent Dopamine Receptor Blocking Activities

A series of some novel N-(1-ethyl-2-pyrrolidinylmethyl)benzamides was synthesized and tested for dopamine receptor blockade in vivo by the ability to block the apomorphine syndrome in the rat.Several compounds were considerably more potent than sulpiride as dopamine receptor blockers and displayed low liability to induce extrapyramidal side effects (catalepsy) in the rat.The blockade of dopamine receptor activity in vivo was mainly confined to the levorotatory isomers having the S absolute configuration.The structure-activity relationships are discussed.