134868-93-2

Usage

Uses

Used in Polymer Industry:
3-(Benzyloxy)-5-hydroxybenzyl Alcohol is used as a monomer for the preparation of amphiphilic homopolymers. Its amphiphilic nature allows it to form polymers with both hydrophilic and hydrophobic properties, making them suitable for a range of applications, such as drug delivery, surface coatings, and materials science.

Upstream product

• 29654-55-5 5-(hydroxymethyl)benzene-1,3-diol 
• 100-44-7 benzyl chloride 
• 100-39-0 benzyl bromide 
• 99-10-5 3,5-Dihydroxybenzoic acid 
• 4142-98-7 ethyl 3,5-dihydroxybenzoate 
• 497069-12-2 ethyl 3-(benzyloxy)-5-hydroxybenzoate 

Downstream Products

• 427901-17-5 2-(3-Benzyloxy-5-hydroxymethyl-phenoxy)-1-phenyl-ethanone 
• 903561-93-3 {3-benzyloxy-5-[3-(phenyl-pyren-1-yl-amino)-benzyloxy]-phenyl}-methanol 
• 129835-67-2 3-benzyloxy-5-hydroxybenzaldehyde 
• 50637-28-0 (3-(benzyloxy)-5-methoxyphenyl)methanol 
• 1246081-74-2 3-benzyloxy-5-((2S)-2-methylbutoxy)-benzyl alcohol 
• 1246081-78-6 9-{[3-benzyloxy-5-((2S)-2-methylbutoxy)benzyloxy]methyl}anthracene 
• 427901-23-3 2-(3-benzyloxy-5-{3-benzyloxy-5-[3-benzyloxy-5-(3-benzyloxy-5-bromomethyl-phenoxymethyl)-phenoxymethyl]-phenoxymethyl}-phenoxy)-1-phenyl-ethanone 
• 427901-22-2 2-(3-Benzyloxy-5-{3-benzyloxy-5-[3-benzyloxy-5-(3-benzyloxy-5-hydroxymethyl-phenoxymethyl)-phenoxymethyl]-phenoxymethyl}-phenoxy)-1-phenyl-ethanone 
• 427901-24-4 3-Benzyloxy-5-{3-benzyloxy-5-[3-benzyloxy-5-(3-benzyloxy-5-hydroxymethyl-phenoxymethyl)-phenoxymethyl]-phenoxymethyl}-phenol 
• 427901-25-5 {3-Benzyloxy-5-[3-benzyloxy-5-(3,5-bis-benzyloxy-benzyloxy)-benzyloxy]-phenyl}-methanol 
• 427901-26-6 C₄₉H₄₃BrO₆ 
• 427901-19-7 2-[3-Benzyloxy-5-(3-benzyloxy-5-hydroxymethyl-phenoxymethyl)-phenoxy]-1-phenyl-ethanone 
• 427901-20-0 2-[3-Benzyloxy-5-(3-benzyloxy-5-bromomethyl-phenoxymethyl)-phenoxy]-1-phenyl-ethanone 
• 427901-21-1 3-Benzyloxy-5-(3-benzyloxy-5-hydroxymethyl-phenoxymethyl)-phenol 

Relevant academic research and scientific papers

A dendrimer chiroptical switch based on the reversible intramolecular photoreaction of anthracene and benzene rings

A series of Frechet-type dendrimers with 9-benzyloxymethylanthracene cores were synthesized and characterized. The chiral source for the dendrimers was an (S)-2-methyl-1-butoxy group in the 3-position of the benzene ring. Irradiation at 366 nm of a dilute

Dendrimer disassembly in the gas phase: A cascade fragmentation reaction of frechet dendrons

The mass spectrometry characterization of Frechet-type dendrons is reported. In order to provide the charges necessary for electrospray ionization, dendrons bearing an OH group at the focal point can be deprotonated and observed in the negative ion mode.

1H-INDOLE-2-CARBOXYLIC ACID DERIVATIVES USEFUL AS PPAR MODULATORS

The present invention relates to certain indole derivatives that are modulators of PPAR, to processes for their preparation, to pharmaceutical compositions containing them and to their use in medicine.

Invertible amphiphilic polymers

Amphiphilic monomeric compounds and corresponding homopolymers and copolymers capable of assembly and invertible configuration in introduction to and change in fluid medium.

Dendrimer analogues of linear molecules to evaluate energy and charge-transfer properties

We have designed and synthesized difunctionalized dendrimers containing two donors in the periphery and an acceptor at the core to serve as scaffolds for comparison with linear analogues to investigate the advantage of dendritic scaffolds for energy and c

Comparison of facially amphiphilic biaryl dendrimers with classical amphiphilic ones using protein surface recognition as the tool

Facially amphiphilic biaryl dendrimers are compared with the more classical benzyl ether amphiphilic dendrimers for molecular recognition, using protein binding as the probe. The protein used for the proposed study is chymotrypsin (ChT). A generation-depe

Homopolymer micelles in heterogeneous solvent mixtures

Amphiphilic homopolymers containing a hydrophilic and a hydrophobic functionality in each monomer unit have been shown to form polar or apolar containers depending on the solvent environment. When presented with a mixture of solvents, these polymeric cont

Invertible amphiphilic homopolymers

Stimuli-responsive polymers and assemblies are viable candidates for the so-called "smart" materials. In this communication, we report a new class of amphiphilic homopolymers that forms micelle-like structures in polar solvents and inverted micelle-like structures in apolar solvents. We demonstrate that these superstructures are the result of the changes in the molecular-level conformations in the monomer. Copyright

Synthesis of difunctionalized dendrimers: An approach to main-chain poly(dendrimers)

Synthesis of benzyl ether dendrimers that are difunctionalized at their peripheries are described. These dendrimers should form the basis for a new class of main-chain dendritic polymers. The steric protection afforded at higher generation during the synt