20032-62-6

Usage

Chemical composition

1,3,5-Benzenetriol, bis(4-methylbenzenesulfonate) is composed of one molecule of 1,3,5-benzenetriol and two molecules of 4-methylbenzenesulfonate.

Structure

1,3,5-Benzenetriol is a benzene derivative with three hydroxyl groups, while 4-methylbenzenesulfonate is a derivative of toluene with a sulfonate group.

Corrosion inhibitor

It is used in water treatment to prevent corrosion.

Catalyst

It serves as a catalyst in organic synthesis.

Stabilizer

It acts as a stabilizer in polymers.

Safety precautions

It is important to handle this chemical with care and follow proper safety protocols, as it can be harmful if ingested or inhaled, and can cause irritation to the skin and eyes.

Hazardous nature

Due to its potential harmful effects, it is classified as a hazardous substance.

Upstream product

• 20032-61-5 1,3,5-tris<(p-toluenesulfonyl)oxy>benzene 
• 108-73-6 3,5-dihydroxyphenol 
• 98-59-9 p-toluenesulfonyl chloride 

Downstream Products

• 89232-61-1 3,5-bis(tosyloxy)phenoxyamine 
• 20032-67-1 4-Nitro-3,5-bis-p-tosyloxy-phenol 
• 918140-64-4 C₂₁H₁₈I₂O₇S₂ 
• 918140-68-8 toluene-4-sulfonic acid 2,4-diiodo-3-methoxy-5-trifluoromethanesulfonyloxy-phenyl ester 

Relevant academic research and scientific papers

First Total Syntheses of Tetracenomycins C and X

The first total syntheses of tetracenomycins C and X were achieved, featuring 1) preparation of a hexasubstituted naphthonitrile oxide by successive benzyne cycloadditions and an oxidative ring-opening reaction; 2) a novel ortho-quinone mono-acetal as the A-ring unit; 3) construction of three contiguous stereogenic centers by an asymmetric benzoin cyclization, an isoxazole oxidation, and a stereoselective reduction.

Nanocompartmentalization of soft materials with three mutually immiscible solvents: Synthesis and self-assembly of three-arm star-polyphiles

We report synthesis, thermotropic, and lyotropic mesomorphism of a family of novel "star-polyphiles": small star-shaped molecules bearing three mutually immiscible arms, hydrophilic (oligoethylene glycol), oleophilic (alkanes), and fluorophilic (perfluorinated alkanes), attached to a central 1,3,5-trihydroxybenzene core. A facile, flexible multistep synthesis giving high-purity yields of 14 distinct members of the family is described, with variable arm lengths, forming crystalline, or various mesostructured gel phases in their neat state at room temperature. Furthermore, we show that specific members of these star-polyphiles can be simultaneously loaded with up to three mutually immiscible solvents, dodecane, perfluoro-nonane, and water, to form liquid crystals and microemulsions with multiple chemically distinct mesoscale compartments. The mesoscale chemical polyfunctionality of these polyphiles, coupled with thermotropic and lyotropic polymorphism, make them promising potential soft materials for a variety of applications, including host matrices for multiple mutually immiscible chemicals and drug delivery.