60785-23-1

Basic information

• Product Name: Benzene, [(2,2-dichloroethyl)thio]-
• CAS NO: 60785-23-1
• Molecular Formula: C8H8Cl2S
• Molecular Weight: 207.124
• Mol File: 60785-23-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzene, [(2,2-dichloroethyl)thio]-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, [(2,2-dichloroethyl)thio]-(60785-23-1)
• EPA Substance Registry System: Benzene, [(2,2-dichloroethyl)thio]-(60785-23-1)

Safety Data

• Hazardous Substances Data: 60785-23-1(Hazardous Substances Data)

Upstream product

• 79-00-5 1,1,2-trichloroethane 
• 108-98-5 thiophenol 
• 156-60-5 trans-1,2-dichloroethylene 

Downstream Products

• 3123-10-2 Phenyl-β,β-dichlorethylsulfon 
• 131575-61-6 (4R,αS)-4-(α-ethoxycarbonyloxybenzyl)-3-phenylsulphonyl-4,5-dihydrofuran 
• 131575-62-7 (4R,αS)-4-(α-methoxymethoxybenzyl)-3-phenylsulphonyl-4,5-dihydrofuran 
• 131616-56-3 (4R,αS)-4-(α-hydroxybenzyl)-3-phenylsulphonyl-4,5-dihydrofuran 
• 131616-55-2 (2S,3R)-2-((E)-2-Benzenesulfonyl-vinyloxymethyl)-3-phenyl-oxirane 
• 58202-75-8 trans β-iodovinyl phenyl sulfone 
• 38238-75-4 (E)-2-chloroethenyl phenyl sulfone 
• 26620-11-1 (E)-2-chlorovinylthiobenzene 

Relevant articles and documents

Novel stereoselective phase transfer catalytic synthesis and some applications of (E)-2-chlorovinylthioarenes and hetarenes

A novel two-step method for the preparation of (E)-2-chlorovinyl-thioarenes (or hetarenes) from thiols and 1,1,2-trichloroethane in the phase transfer catalytic systems solid K2CO3/solid KI/18-crown-6/xylene and solid KOH/18-crown-6/

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.