70197-34-1

Basic information

• Product Name: (Z)-1-n-Butyl-2-phenylthioethene
• Synonyms: (Z)-1-n-Butyl-2-phenylthioethene
• CAS NO: 70197-34-1
• Molecular Weight: 192.325
• Mol File: 70197-34-1.mol
• Article Data: 13

Chemical Properties

• CAS DataBase Reference: (Z)-1-n-Butyl-2-phenylthioethene(CAS DataBase Reference)
• NIST Chemistry Reference: (Z)-1-n-Butyl-2-phenylthioethene(70197-34-1)
• EPA Substance Registry System: (Z)-1-n-Butyl-2-phenylthioethene(70197-34-1)

Safety Data

• Hazardous Substances Data: 70197-34-1(Hazardous Substances Data)

Upstream product

• 110-62-3 pentanal 
• 127894-31-9 1-phenylthio-1-hexyne 
• 108-98-5 thiophenol 
• 693-02-7 hex-1-yne 
• 26620-11-1 (E)-2-chlorovinylthiobenzene 
• 17101-71-2 Z-β-bromovinyl phenyl sulfide 
• 15366-08-2 s-butylmagnesium chloride 
• 693-03-8 n-butyl magnesium bromide 
• 13154-12-6 (Z)-1-bromohex-1-ene 
• 931-59-9 benzenesulfenyl chloride 
• 2973-86-6 lithium thiophenoxide 

Downstream Products

• 7433-78-5 cis-5-decene 
• 7433-56-9 (E)-5-decene 

Relevant articles and documents

Catalytic conversion of alkynes to α-vinyl sulfides mediated by carbene-linker-carbene (CXC) rhodium and iridium complexes

The catalytic activity of a set of mono- and bimetallic Rh(i) and Ir(i) complexes bearing carbene-linker-carbene (CXC) bis-triazolylidene ligands (with X = O, N) coordinated in a bridging or chelating fashion was evaluated in the hydrothiolation of alkyne

Stereoselective hydrozirconation of alkynylsulfide and regioselective synthesis of haloalkenyl sulfide via electrophile-switched halogenation of thioalkenyl zirconocene

Stereoselective preparation of alkenyl sulfide was carried out via syn-hydrozirconation of the alkynyl sulfide. Regiochemistry of halogenation of the thioalkenyl zirconocene could be switched by different halides. α-Chloroalkenyl sulfide or β-haloalkenyl

Water-promoted regioselective hydrothiolation of alkynes

Water promotes hydrothiolation of unactivated alkynes efficiently without any catalyst or additive. The reaction at room temperature furnishes vinyl sulfides with high regioselectivity via anti-Markovnikov addition. The terminal al- kynes provide dithiola