160661-43-8

Basic information

• Product Name: 1,2-dibromo-1-phenylsulfanyl-ethane
• Synonyms: 1,2-dibromo-1-phenylsulfanyl-ethane
• CAS NO: 160661-43-8
• Molecular Weight: 296.026
• Mol File: 160661-43-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1,2-dibromo-1-phenylsulfanyl-ethane(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-dibromo-1-phenylsulfanyl-ethane(160661-43-8)
• EPA Substance Registry System: 1,2-dibromo-1-phenylsulfanyl-ethane(160661-43-8)

Safety Data

• Hazardous Substances Data: 160661-43-8(Hazardous Substances Data)

Upstream product

• 20451-53-0 Phenyl vinyl sulfoxide 
• 1822-73-7 phenylthioethylene 

Downstream Products

• 130659-35-7 tert-Butyl-dimethyl-((E)-3-phenylsulfanyl-3-tributylstannanyl-allyloxy)-silane 
• 130659-35-7 tert-Butyl-dimethyl-((E)-3-phenylsulfanyl-3-tributylstannanyl-allyloxy)-silane 
• 130659-39-1 tert-Butyl-((Z)-3-iodo-3-phenylsulfanyl-allyloxy)-dimethyl-silane 
• 130659-37-9 tert-Butyl-((E)-3-iodo-3-phenylsulfanyl-allyloxy)-dimethyl-silane 
• 130659-38-0 (Z)-3-Iodo-3-phenylsulfanyl-prop-2-en-1-ol 
• 130659-38-0 (E)-3-Iodo-3-phenylsulfanyl-prop-2-en-1-ol 
• 89005-19-6 3-(phenylsulfanyl)propargyl alcohol 
• 130659-41-5 (Z)-6-(tert-Butyl-dimethyl-silanyloxy)-3-methyl-4-phenylsulfanyl-1-trimethylsilanyl-hex-4-en-1-yn-3-ol 
• 130659-40-4 (Z)-1-iodo-1-phenylthio-3-(tetrahydropyran-2-yl)oxy-1-propene 
• 130659-33-5 2-((3-(phenylthio)prop-2-yn-1-yl)oxy)tetrahydro-2H-pyran 
• 130659-42-6 (Z)-4-Methyl-3-phenylsulfanyl-hex-2-en-5-yne-1,4-diol 
• 130659-36-8 tert-Butyl-dimethyl-((Z)-3-phenylsulfanyl-allyloxy)-silane 
• 130659-34-6 tert-butyldimethyl((3-(phenylthio)prop-2-yn-1-yl)oxy)silane 
• 20408-25-7 trans-β-Bromovinyl phenyl sulfone 

Relevant articles and documents

Stereoselective construction and synthetic applications of phenylthio substituted iodoolefins

(E)- and (Z)-Phenylthio substituted iodoolefins 1 and 2 have been synthesized stereoselectively via lower order stannylcuprate addition to and hydroalumination of appropriate alkyne precursors. Their utility in model studies on the synthesis of calichemic

NUCLEOPHILIC REACTION AT A VINYL CENTER. XXII. SYNTHESIS AND NUCLEOPHILIC VINYLIC SUBSTITUTION IN E-β-FLUOROVINYL ARYL SULFONES

The reaction of potassium fluoride with E-β-bromovinyl aryl sulfones in the presence of 18-crown-6-ether leads to a mixture of the sulfones XC6H4SO2CH2CHF2 and E-XC6H4SO2CH=CHF, the ratio of which decreases in the order X=CH3, H, Cl, NO2.The kinetics of n