41856-37-5

Basic information

• Product Name: 1-bromo-2-phenylsulphonylstyrene
• Synonyms: 1-bromo-2-phenylsulphonylstyrene
• CAS NO: 41856-37-5
• Molecular Weight: 323.21
• Mol File: 41856-37-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1-bromo-2-phenylsulphonylstyrene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-bromo-2-phenylsulphonylstyrene(41856-37-5)
• EPA Substance Registry System: 1-bromo-2-phenylsulphonylstyrene(41856-37-5)

Safety Data

• Hazardous Substances Data: 41856-37-5(Hazardous Substances Data)

Upstream product

• 98-09-9 benzenesulfonyl chloride 
• 536-74-3 phenylacetylene 
• 2297-65-6 benzenesulfonyl bromide 

Downstream Products

• 5324-64-1 2-(benzenesulfonyl)ethynylbenzene 
• 3406-03-9 2-(phenylsulfonyl)acetophenone 
• 82211-05-0 1-phenyl-2-(phenylsulfonyl)-2-(phenylthio)ethan-1-one 
• 131575-93-4 (2S,3S,4R,αS)-2-phenyl-3-phenylsulphonyl-4-(α-ethoxycarbonyloxybenzyl)tetrahydrofuran 
• 131575-67-2 (4R,αS)-2-phenyl-3-phenylsulphonyl-4-(α-ethoxycarbonyloxybenzyl)-4,5-dihydrofuran 
• 131575-68-3 (4R,αS)-2-phenyl-3-phenylsulphonyl-4-(α-methoxymethyloxybenzyl)-4,5-dihydrofuran 
• 131575-64-9 (2S,3R)-2-((E)-2-Benzenesulfonyl-1-phenyl-vinyloxymethyl)-3-phenyl-oxirane 
• 131575-63-8 (2S,3R)-2-((Z)-1-Benzenesulfonyl-2-phenyl-vinyloxymethyl)-3-phenyl-oxirane 
• 131575-92-3 (2S,3S,4R,αS)-4-(α-hydroxybenzyl)-2-phenyl-3-phenylsulphonyltetrahydrofuran 
• 131575-65-0 (4R,αS)-4-(α-hydroxybenzyl)-2-phenyl-3-phenylsulphonyl-4,5-dihydrofuran 
• 131575-66-1 (2R,3S)-2-Phenyl-3-phenylethynyloxymethyl-oxirane 

Relevant articles and documents

Approaches to 2,6-Diaryl-3,7-DioxabicycloOctane Lignans via Asymmetric Synthesis of Dihydro- and Tetrahydro-furan Derivatives

Cyclisation of chiral non-racemic phenylsulphonylvinyl epoxy ethers, produced using the Sharpless epoxidation reaction, has been used to prepare a series of enantiomerically enriched 2-aryl-4-(α-hydroxybenzyl)-4,5-dihydrofuran derivatives.Reduction of these compounds using triethylsilane and BF3-diethyl ether gave the corresponding tetrahydrofuran derivatives stereoselectively.Attempts to convert either the dihydro- or tetrahydro-furan derivatives into lignans belonging to the 2,6-diaryl-3,7-dioxabicyclooctane series so far proved unsuccessful.