52959-28-1

Basic information

• Product Name: diMethyl 4,6-dihydroxyisophthalate
• Synonyms: diMethyl 4,6-dihydroxyisophthalate;Dimethyl 2,4-Dihydroxybenzene-1,5-Dicarboxylate;4,6-Dihydroxy-1,3-benzenedicarboxylic acid dimethyl ester;4,6-dihydroxy-, 1,3-dimethyl ester
• CAS NO: 52959-28-1
• Molecular Formula: C₁₀H₁₀O₆
• Molecular Weight: 226.1828
• EINECS: -0
• Mol File: 52959-28-1.mol
• Article Data: 11

Chemical Properties

• Appearance: /
• CAS DataBase Reference: diMethyl 4,6-dihydroxyisophthalate(CAS DataBase Reference)
• NIST Chemistry Reference: diMethyl 4,6-dihydroxyisophthalate(52959-28-1)
• EPA Substance Registry System: diMethyl 4,6-dihydroxyisophthalate(52959-28-1)

Safety Data

• Hazardous Substances Data: 52959-28-1(Hazardous Substances Data)

Usage

General Description

DiMethyl 4,6-dihydroxyisophthalate is a chemical compound with the molecular formula C10H10O6. It belongs to the family of isophthalates, which are commonly used as building blocks for various polymers and resins. DiMethyl 4,6-dihydroxyisophthalate is a diester of isophthalic acid, and it contains two methyl groups and two hydroxyl groups. diMethyl 4,6-dihydroxyisophthalate is often utilized in the production of polyester resins, engineering plastics, and adhesives. It is known for its high thermal and chemical resistance, making it suitable for a wide range of industrial applications. Additionally, it is considered to be a versatile building block for the synthesis of complex organic molecules in the field of organic chemistry.

Upstream product

• 186581-53-3 diazomethane 
• 19829-74-4 4,6-dihydroxyisophthalic acid 
• 591-27-5 m-Hydroxyaniline 
• 15540-79-1 4-amino-6-hydroxyisophthalic acid 
• 7168-99-2 4,6-dimethoxy-isophthalic acid 
• 108-46-3 recorcinol 
• 77-78-1 dimethyl sulfate 
• 67-56-1 methanol 

Downstream Products

• 14965-05-0 4,6-dimethoxyisophthalic acid dimethyl ester 
• 15931-89-2 2.5-Bis--terephthalsaeure-dimethylester 
• 231954-15-7 4,6-di(isobutoxy)isophthalic acid dimethyl ester 
• 939374-70-6 C₂₂H₃₄O₁₀ 
• 13936-92-0 1-(2,6-dihydroxyphenyl)-2-phenylethanone 
• 15926-86-0 4,6-Bis--isophthalsaeure-dimethylester 
• 15926-88-2 4,6-Bis--isophthalsaeure-dimethylester 
• 4498-97-9 4,6-Bis--isophthalsaeure-dimethylester 
• 4021-15-2 4,6-Bis--isophthalsaeure-dimethylester 
• 15926-84-8 4,6-Bis--isophthalsaeure-dimethylester 
• 15926-78-0 4,6-Bis--isophthalsaeure-dimethylester 
• 13937-27-4 2,6-dihydroxy-α-oxo-bibenzyl-3,5-dicarboxylic acid dimethyl ester 
• 874210-29-4 4,6-bis{2-[2-(2-methoxyethoxy)ethoxy]ethoxy}isophthalic acid dimethyl ester 
• 787629-25-8 4,6-dioctyloxy-1,3-dibenzoic acid dihydrazide 

Relevant articles and documents

Polyhydrazide-Based Organic Nanotubes as Efficient and Selective Artificial Iodide Channels

Reported herein is a series of pore-containing polymeric nanotubes based on a hydrogen-bonded hydrazide backbone. Nanotubes of suitable lengths, possessing a hollow cavity of about a 6.5 ? diameter, mediate highly efficient transport of diverse types of anions, rather than cations, across lipid membranes. The reported polymer channel, having an average molecular weight of 18.2 kDa and 3.6 nm in helical height, exhibits the highest anion-transport activities for iodide (EC50=0.042 μm or 0.028 mol % relative to lipid), whcih is transported 10 times more efficiently than chlorides (EC50=0.47 μm). Notably, even in cholesterol-rich environment, iodide transport activity remains high with an EC50 of 0.37 μm. Molecular dynamics simulation studies confirm that the channel is highly selective for anions and that such anion selectivity arises from a positive electrostatic potential of the central lumen rendered by the interior-pointing methyl groups.

CAVITY-CONTAINING OLIGOMERS AND POLYMERS EFFECTIVE IN CRYOPRESERVATION

The present invention provides compositions and methods for cryopreservation utilizing aromatic cavity-containing oligomers and polymers that contain structural motifs capable of shape-inducing intramolecular bonding to form cavities. The cavity-containin

Highly Ordered Nanoporous Films from Supramolecular Diblock Copolymers with Hydrogen-Bonding Junctions

We designed efficient precursors that combine complementary associative groups with exceptional binding affinities and thiocarbonylthio moieties enabling precise RAFT polymerization. Well defined PS and PMMA supramolecular polymers with molecular weights up to 30 kg mol?1are synthesized and shown to form highly stable supramolecular diblock copolymers (BCPs) when mixed, in non-polar solvents or in the bulk. Hierarchical self-assembly of such supramolecular BCPs by thermal annealing affords morphologies with excellent lateral order, comparable to features expected from covalent diblock copolymer analogues. Simple washing of the resulting materials with protic solvents disrupts the supramolecular association and selectively dissolves one polymer, affording a straightforward process for preparing well-ordered nanoporous materials without resorting to crosslinking or invasive chemical degradations.