134868-93-2

Basic information

• Product Name: 3-(Benzyloxy)-5-hydroxybenzyl Alcohol
• Synonyms: 3-(Benzyloxy)-5-hydroxybenzyl Alcohol;3-(benzyloxy)-5-(hydroxymethyl)phenol
• CAS NO: 134868-93-2
• Molecular Formula: C₁₄H₁₄O₃
• Molecular Weight: 230.25916
• Product Categories: Aromatics;Intermediates & Fine Chemicals;Metabolites & Impurities;Pharmaceuticals;Aromatics, Metabolites & Impurities, Pharmaceuticals, Intermediates & Fine Chemicals
• Mol File: 134868-93-2.mol
• Article Data: 9

Chemical Properties

• Appearance: /
• Solubility: Dichloromethane, Ethyl Acetate
• CAS DataBase Reference: 3-(Benzyloxy)-5-hydroxybenzyl Alcohol(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(Benzyloxy)-5-hydroxybenzyl Alcohol(134868-93-2)
• EPA Substance Registry System: 3-(Benzyloxy)-5-hydroxybenzyl Alcohol(134868-93-2)

Safety Data

• Hazardous Substances Data: 134868-93-2(Hazardous Substances Data)

Usage

Description

3-(Benzyloxy)-5-hydroxybenzyl Alcohol is an organic compound characterized by its brown oil appearance. It is known for its unique chemical structure, which features a benzyloxy group at the 3-position and a hydroxyl group at the 5-position on a benzene ring. 3-(Benzyloxy)-5-hydroxybenzyl Alcohol is of interest due to its potential applications in various industries.

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

• 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 
• 758724-74-2 (3-benzyloxy-5-vinyl-phenoxy)-acetic acid tert-butyl ester 
• 758724-73-1 (3-benzyloxy-5-formyl-phenoxy)-acetic acid tert-butyl ester 
• 906457-98-5 [6-benzyloxy-3',5'-bis-(3-benzyloxy-5-tert-butoxycarbonylmethoxy-benzyloxy)-4-hydroxymethyl-biphenyl-2-yloxy]-acetic acid tert-butyl ester 
• 906457-99-6 [6-benzyloxy-3',5'-bis-(3-benzyloxy-5-tert-butoxycarbonylmethoxy-benzyloxy)-4-bromomethyl-biphenyl-2-yloxy]-acetic acid tert-butyl ester 
• 906457-97-4 (3-benzyloxy-5-bromomethyl-phenoxy)-acetic acid tert-butyl ester 
• 903561-93-3 {3-benzyloxy-5-[3-(phenyl-pyren-1-yl-amino)-benzyloxy]-phenyl}-methanol 
• 758724-72-0 (3-benzyloxy-5-hydroxymethyl-phenoxy)-acetic acid tert-butyl ester 
• 480447-32-3 2-[3-(3-benzyloxy-5-hydroxymethyl-phenoxymethyl)-phenoxy]-1-phenyl-ethanone 
• 427901-19-7 2-[3-Benzyloxy-5-(3-benzyloxy-5-hydroxymethyl-phenoxymethyl)-phenoxy]-1-phenyl-ethanone 
• 427901-17-5 2-(3-Benzyloxy-5-hydroxymethyl-phenoxy)-1-phenyl-ethanone 

Relevant articles and documents

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

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.

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