184219-30-5

Basic information

• Product Name: C₄₉H₄₃ClO₆
• Synonyms: C₄₉H₄₃ClO₆
• CAS NO: 184219-30-5
• Molecular Weight: 763.33
• Mol File: 184219-30-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: C₄₉H₄₃ClO₆(CAS DataBase Reference)
• NIST Chemistry Reference: C₄₉H₄₃ClO₆(184219-30-5)
• EPA Substance Registry System: C₄₉H₄₃ClO₆(184219-30-5)

Safety Data

• Hazardous Substances Data: 184219-30-5(Hazardous Substances Data)

Upstream product

• 100-44-7 benzyl chloride 
• 67093-27-0 3,5-dibenzyloxybenzyl chloride 
• 29654-55-5 5-(hydroxymethyl)benzene-1,3-diol 
• 24131-31-5 3,5-dibenzyloxybenzyl alcohol 
• 129536-40-9 [3,5-Bis-(3,5-bis-benzyloxy-benzyloxy)-phenyl]-methanol 

Downstream Products

• 137472-16-3 [3,5-bis[[3,5-bis[[3,5-bis(phenylmethoxy)phenyl]methoxy]phenyl]methoxy]phenyl]methyl alcohol 
• 1032464-79-1 C₆₁H₅₄O₈ 
• 278610-81-4 3-[3,5-Bis-(3,5-bis-benzyloxy-benzyloxy)-benzyloxy]-5-hydroxymethyl-phenol 
• 1246081-80-0 9-[(3-{3,5-bis[3,5-bis(benzyloxy)benzyloxy]benzyloxy}-5-((2S)-2-methylbutoxy)benzyloxy)methyl]anthracene 

Relevant articles and documents

Synthesis of dendritic phenol ether derivatives with a naphthalene core

A series of dendritic phenol ether derivatives with a naphthalene core were synthesized by the Williamson reaction as a coupling reaction between 1-hydroxymethylnaphthalene and polyether-based dendritic fragments in the presence of phase-transfer catalyst and alkali. The modified method for chlorination of dendritic benzyl alcohol was also developed using PPh3 and CCl4 as reagents and CH2Cl2/CCl4 as solvent. Copyright Taylor & Francis Group, LLC.

Dendritic initiators for "living" radical polymerizations: A versatile approach to the synthesis of dendritic-linear block copolymers

The first use of polyether dendrons as macromolecular initiators for the controlled free radical polymerization of vinyl monomers has been demonstrated. Dendrons containing either a single benzylic TEMPO or halide functionality at their focal point have b