570-02-5

Basic information

• Product Name: 2,4,6-Trimethoxybenzoic acid
• Synonyms: 2,4,6-Trimethoxybenzoic;LABOTEST-BB LT00848114;2,4,6-TRIMETHOXYBENZOIC ACID;RARECHEM AL BO 0029;PHLOROGLUCINOL CARBOXYLIC ACIDRIMETHYL ETHER;PHLOROGLUCINOL CARBOXYLIC ACID TRIMETHYL ETHER;2,4,6-trimethoxy-benzoicaci;2,4,6-Trimethxoybenzoic acid
• CAS NO: 570-02-5
• Molecular Formula: C₁₀H₁₂O₅
• Molecular Weight: 212.2
• EINECS: 209-325-4
• Product Categories: Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts;Organic acids
• Mol File: 570-02-5.mol
• Article Data: 11

Chemical Properties

• Melting Point: 158°C (dec.)
• Boiling Point: 350.6 °C at 760 mmHg
• Flash Point: 137.4 °C
• Appearance: /
• Density: 1.219 g/cm³
• Vapor Pressure: 1.62E-05mmHg at 25°C
• Refractive Index: 1.523
• Solubility: soluble in Methanol
• PKA: 4.25±0.10(Predicted)
• BRN: 1972294
• CAS DataBase Reference: 2,4,6-Trimethoxybenzoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4,6-Trimethoxybenzoic acid(570-02-5)
• EPA Substance Registry System: 2,4,6-Trimethoxybenzoic acid(570-02-5)

Safety Data

• Safety Statements: 22-24/25
• TSCA: Yes
• Hazardous Substances Data: 570-02-5(Hazardous Substances Data)

Usage

Uses

2,4,6-Trimethoxybenzoic Acid is a useful research chemical for organic synthesis and other chemical processes.

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

Upstream product

• 830-79-5 2,4,6-trimethoxybenzaldehyde 
• 29723-28-2 methyl 2,4,6-trimethoxybenzoate 
• 105338-30-5 methyl 2,4,6-trimethoxyphenylglyoxylate 
• 51116-92-8 methyl 4,6-dimethoxysalicylate 
• 77-78-1 dimethyl sulfate 
• 314-98-7 2,2,2-trifluoro-1-(2,4,6-trimethoxyphenyl)ethan-1-one 
• 336621-34-2 2,4,6-trimethoxy-benzoic acid 1,1-diethyl-propyl ester 
• 42833-84-1 2,4,6-trimethoxybenzoyl chloride 
• 621-23-8 1,2,3-trimethoxybenzene 
• 124-38-9 carbon dioxide 
• 61040-78-6 2,4,6-trimethoxybenzyl alcohol 
• 108-73-6 3,5-dihydroxyphenol 
• 68-12-2 N,N-dimethyl-formamide 

Downstream Products

• 109394-41-4 2,4,6-trimethoxy-benzoic acid-(2-dimethylamino-ethyl ester) 
• 29723-28-2 methyl 2,4,6-trimethoxybenzoate 
• 89075-21-8 2-(2,4,6-Trimethoxy-phenyl)-3H-imidazo[4,5-c]pyridine 
• 621-23-8 1,2,3-trimethoxybenzene 
• 1188927-66-3 C₁₆H₂₂O₅ 
• 1188927-62-9 C₁₆H₂₄O₅ 
• 1228802-99-0 2,2'-((4-(trifluoromethyl)phenyl)methylene)bis(1,3,5-trimethoxybenzene) 
• 1228802-90-1 N-((2-bromo-4-fluorophenyl)(2,4,6-trimethoxyphenyl)methyl)-4-methylbenzenesulfonamide 
• 1228802-86-5 4-methyl-N-((4-nitrophenyl)(2,4,6-trimethoxyphenyl)methyl)benzenesulfonamide 
• 1228802-98-9 2,2'-((2-bromo-4-fluorophenyl)methylene)bis(1,3,5-trimethoxybenzene) 
• 1228802-97-8 2,2'-((2-chlorophenyl)methylene)bis(1,3,5-trimethoxybenzene) 
• 1228802-96-7 2,2'-((2,4-dichlorophenyl)methylene)bis(1,3,5-trimethoxybenzene) 
• 1228802-91-2 N-((2-chlorophenyl)(2,4,6-trimethoxyphenyl)methyl)-4-methylbenzenesulfonamide 
• 1228802-88-7 N-((2,4-dichlorophenyl)(2,4,6-trimethoxyphenyl)methyl)-4-methylbenzenesulfonamide 

Relevant articles and documents

Efficient and convenient oxidation of aldehydes and ketones to carboxylic acids and esters with H2O2 catalyzed by Co4HP2Mo15V3O62 in ionic liquid [TEBSA][BF4]

A simple, efficient, and eco-friendly procedure for the oxidation of aldehydes and ketones to carboxylic acids and esters with H2O2 catalyzed by Co4HP2Mo15V3O62 in ionic liquid [TEBSA][BF4] has been developed. This atom-economical protocol affords the target products in good to high yields. The products can be separated by a simple extraction with organic solvent, and the catalytic system can be recycled and reused without loss of catalytic activity. Additionally, the possible mechanism of oxidation in the catalytic system is proposed. This journal is

Cu(II) bromide catalyzed oxidation of aldehydes and alcohols

A variety of aromatic, aliphatic and conjugated aldehydes and alcohols were transformed to the corresponding carboxylic acids and ketones with a quantitative conversion in high yields with 70% t-BuOOH solution in water in the presence of catalytic (5 mol%) amounts of CuBr2 under room temperature conditions. The conversion of 4-methoxybenzaldehyde to 4-methoxybenzoic acid is extremely facile in MeCN at ambient temperature in the presence of 5 mol% CuBr2 and 2 equiv. 70% t-BuOOH (water) as the oxidant. Oxidation with t-BuOOH (water) alone in MeCN was found to be negligible. The scope of our catalytic system is applicable for a wide range of aromatic, conjugated and aliphatic substrates. These aldehydes were converted to the corresponding carboxylic acids in good isolated yields in reasonable times. It is pertinent to mention here that mild halogenic oxidants like hypochlorites, chlorites and NBS are not suitable for substrates with electron-rich aromatic rings, olefinic bonds and secondary hydroxyl groups. Substitutions at different positions on the phenyl ring do not hinder the reaction, although the reaction time is affected. Oxidation of α,β unsaturated derivatives resulted in the formation of the expected acid in good yield. In addition, the transformation of secondary alcohols to ketones is extremely facile. No recemization was observed for menthone. This method possesses a wide range of capabilities since it can be used with other functional groups which may not tolerate oxidative conditions, involves fairly simple method for work-up, exhibits chemoselectivity and proceeds under ambient conditions. The resulting products are obtained in good yields within reasonable time.