84574-53-8

Basic information

• Product Name: (2S,3S,5R,6R)-2,3,5,6-Tetrakis-(2-chloro-phenyl)-[1,4]dioxane
• Synonyms: (2S,3S,5R,6R)-2,3,5,6-Tetrakis-(2-chloro-phenyl)-[1,4]dioxane
• CAS NO: 84574-53-8
• Molecular Weight: 530.278
• Mol File: 84574-53-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (2S,3S,5R,6R)-2,3,5,6-Tetrakis-(2-chloro-phenyl)-[1,4]dioxane(CAS DataBase Reference)
• NIST Chemistry Reference: (2S,3S,5R,6R)-2,3,5,6-Tetrakis-(2-chloro-phenyl)-[1,4]dioxane(84574-53-8)
• EPA Substance Registry System: (2S,3S,5R,6R)-2,3,5,6-Tetrakis-(2-chloro-phenyl)-[1,4]dioxane(84574-53-8)

Safety Data

• Hazardous Substances Data: 84574-53-8(Hazardous Substances Data)

Upstream product

• 611-17-6 1-bromomethyl-2-chlorobenzene 
• 89-98-5 2-chloro-benzaldehyde 
• 17849-38-6 2-Chlorobenzyl alcohol 
• 95-49-8 2-methylchlorobenzene 
• 71776-58-4 (1R,2S)-1,2-bis-(2-chloro-phenyl)-ethane-1,2-diol 

Relevant articles and documents

PHOTOCHEMICAL REACTION OF ALCOHOLS - II. IRRADIATION OF AROMATIC ALCOHOLS

The UV irradiation of aromatic alcohols leads to the formation of several products: carbonyl compounds, ethers, α-glycols and tetra-aryl-1,4-dioxanes.The photoformation of α-glycols is qualitatively and quantitatively compared to the photoreduction of the carbonyl compounds.It is noteworthy that the glycols are formed with a stereochemistry very different depending upon whether the substrate is an alcohol or a carbonyl compound.The structure, configuration and conformation of the 1,4-dioxanes obtained are studied as well as their origin.Other aspects of the photochemistry of the alcohols are analyzed using hydroperoxides as model substrates.