278610-81-4

Basic information

• Product Name: 3-[3,5-Bis-(3,5-bis-benzyloxy-benzyloxy)-benzyloxy]-5-hydroxymethyl-phenol
• Synonyms: 3-[3,5-Bis-(3,5-bis-benzyloxy-benzyloxy)-benzyloxy]-5-hydroxymethyl-phenol
• CAS NO: 278610-81-4
• Molecular Weight: 867.008
• Mol File: 278610-81-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 3-[3,5-Bis-(3,5-bis-benzyloxy-benzyloxy)-benzyloxy]-5-hydroxymethyl-phenol(CAS DataBase Reference)
• NIST Chemistry Reference: 3-[3,5-Bis-(3,5-bis-benzyloxy-benzyloxy)-benzyloxy]-5-hydroxymethyl-phenol(278610-81-4)
• EPA Substance Registry System: 3-[3,5-Bis-(3,5-bis-benzyloxy-benzyloxy)-benzyloxy]-5-hydroxymethyl-phenol(278610-81-4)

Safety Data

• Hazardous Substances Data: 278610-81-4(Hazardous Substances Data)

Upstream product

• 29654-55-5 5-(hydroxymethyl)benzene-1,3-diol 
• 184219-30-5 C₄₉H₄₃ClO₆ 
• 129536-40-9 [3,5-Bis-(3,5-bis-benzyloxy-benzyloxy)-phenyl]-methanol 
• 24131-32-6 3,5-bis(benzyloxy)benzyl bromide 
• 24131-31-5 3,5-dibenzyloxybenzyl alcohol 
• 129536-41-0 3,5-bis[3,5-bis(benzyloxy)benzyloxy]benzyl bromide 
• 246512-25-4 methanesulfonic acid 3,5-bis-(3,5-bis-benzyloxy-benzyloxy)-benzyl ester 
• 80457-61-0 methanesulfonyl 3,5-dibenzyloxybenzyl alcohol 

Downstream Products

• 1246081-76-4 3-{3,5-bis[3,5-bis(benzyloxy)benzyloxy]benzyloxy}-5-((2S)-2-methylbutoxy)-benzyl alcohol 
• 1246081-80-0 9-[(3-{3,5-bis[3,5-bis(benzyloxy)benzyloxy]benzyloxy}-5-((2S)-2-methylbutoxy)benzyloxy)methyl]anthracene 
• 134868-82-9 4-[3-Benzyloxy-5-(3-(3,5-bis-benzyloxy-benzyloxy)-5-{3-[3,5-bis-(3,5-bis-benzyloxy-benzyloxy)-benzyloxy]-5-hydroxymethyl-phenoxymethyl}-phenoxymethyl)-phenoxymethyl]-benzonitrile 

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

Polymers with Controlled Molecular Architecture: Control of Surface Functionality in the Synthesis of Dendritic Hyperbranched Macromolecules using the Convergent Approach

The synthesis of unsymmetrically or non-uniformly surface-functionalized dentritic macromolecules using a stepwise convergent-growth approach is described.By stepwise alkylation of the monomer unit, 3,5-dihydroxybenzyl alcohol, with unsubstituted and subs