60785-27-5

Basic information

• Product Name: {[(Z)-2-chloroethenyl]sulfanyl}benzene
• Synonyms: {[(Z)-2-chloroethenyl]sulfanyl}benzene
• CAS NO: 60785-27-5
• Molecular Weight: 170.663
• Mol File: 60785-27-5.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: {[(Z)-2-chloroethenyl]sulfanyl}benzene(CAS DataBase Reference)
• NIST Chemistry Reference: {[(Z)-2-chloroethenyl]sulfanyl}benzene(60785-27-5)
• EPA Substance Registry System: {[(Z)-2-chloroethenyl]sulfanyl}benzene(60785-27-5)

Safety Data

• Hazardous Substances Data: 60785-27-5(Hazardous Substances Data)

Upstream product

• 1822-73-7 phenylthioethylene 
• 108-98-5 thiophenol 
• 86240-69-9 (1,2-Dichloro-ethylsulfanyl)-benzene 
• 540-59-0 1,2-Dichloroethylene 
• 156-59-2 cis-1,2-Dichloroethylene 
• 930-69-8 sodium thiophenolate 
• 156-60-5 trans-1,2-dichloroethylene 
• 706-02-5 (2E)-3-(phenylthio)acrylic acid 
• 706-01-4 (2Z)-3-(phenylthio)acrylic acid 

Downstream Products

• 7392-12-3 (Z)-1-(phenylthio)-2-(phenylseleno)ethylene 
• 105590-38-3 (Z)-β-styryl,(Z)-2-phenylthio-1-ethenyl selenide 
• 95391-86-9 (Z)-(phenylthio)ethenyl methyl selenide 
• 105590-37-2 (E)-β-styryl,(Z)-2-phenylthio-1-ethenyl selenide 
• 100155-64-4 ((Z)-2-Ethylselanyl-vinylsulfanyl)-benzene 
• 37530-86-2 1-phenylsulfonyl-2-(phenylthio)ethene 
• 55485-71-7 cis-1-benzenesulfonyl-2-phenylsulfanyl-ethylene 
• 99186-04-6 2-ethoxyvinyl phenyl sulfide 
• 71022-63-4 cis-1-benzenesulfonyl-2-chloro-ethylene 
• 6228-98-4 phenylthioacetylene 
• 18893-62-4 cis-1,2-bis-phenylsulfanyl-ethylene 

Relevant articles and documents

Olefin cross-metathesis with vinyl halides

The first successful example of olefin cross-metathesis with chloroalkenes is reported. The Royal Society of Chemistry.

HIGH-TEMPERATURE ORGANIC SYNTHESIS. XXXIX. GAS-PHASE REACTION OF THIOPHENOL WITH 1,2-DICHLOROETHENE

Thiophenol reacts with 1,2-dichloroethene (a 3:1 mixture of E and Z isomers) in the gas phase at 400-550 deg C forming phenyl β-chlorovinyl sulfide (E and Z isomers, 1:1) with an overall yield of up to 84percent.The products from its further thermal transformations are benzothiophene. 3-chlorobenzothiophene, 1,2-bis(phenylthio)ethene (a mixture of stereoisomers), and 3-phenylthiobenzothiophene