16906-37-9

Usage

Uses

Used in Organic Synthesis:
CIS-1,2-BIS(BENZYLTHIO)ETHYLENE is used as a building block for the synthesis of organic molecules, leveraging its unique structure and reactivity to create a variety of compounds with diverse properties and applications.
Used in Coordination Chemistry:
CIS-1,2-BIS(BENZYLTHIO)ETHYLENE is used as a ligand for the formation of stable complexes with transition metals. Its ability to chelate metals enhances the stability and reactivity of these complexes, making BTE a valuable component in coordination chemistry.
Used in Catalytic Reactions:
CIS-1,2-BIS(BENZYLTHIO)ETHYLENE is used as a catalyst or a catalyst precursor in various chemical reactions. Its metal complexes can facilitate and enhance the rates of reactions, improving the efficiency and selectivity of synthetic processes.
Used in Materials Science:
CIS-1,2-BIS(BENZYLTHIO)ETHYLENE is used in the development of new materials with unique properties. Its ability to form stable complexes and its structural features make it a promising candidate for applications in materials science, such as the creation of novel polymers, sensors, or electronic devices.
Used in Research and Development:
CIS-1,2-BIS(BENZYLTHIO)ETHYLENE is used as a versatile chemical in various fields of research and development. Its potential applications in catalysis, chelating, materials science, and organic synthesis make it an invaluable tool for scientists and researchers working on innovative projects and discoveries.

InChI:InChI=1/C16H16S2/c1-3-7-15(8-4-1)13-17-11-12-18-14-16-9-5-2-6-10-16/h1-12H,13-14H2/b12-11-

Upstream product

• 75-35-4 1,1-Dichloroethylene 
• 3492-64-6 sodium benzylmercaptide 
• 150-60-7 dibenzyl disulphide 
• 540-59-0 1,2-Dichloroethylene 

Downstream Products

• 788-26-1 ({[(E)-2-(benzylsulfanyl)ethenyl]sulfanyl}methyl)benzene 
• 141170-33-4 (1S,4R,5R,6R)-5,6-Bis-phenylmethanesulfonyl-bicyclo[2.2.1]hept-2-ene 
• 141126-32-1 (1S,2S,3S,5R,6R,7S,9R)-2-Bromo-9-phenylmethanesulfonyl-4-oxa-5-thia-tricyclo[4.2.1.0^3,7]nonane 5-oxide 
• 141126-33-2 (1S,2S,3S,6R,7S,9R)-2-Bromo-9-phenylmethanesulfonyl-4-oxa-5-thia-tricyclo[4.2.1.0^3,7]nonane 5,5-dioxide 
• 141126-35-4 (E)-1,2-bis-(benzylsulphonyl)ethylene 
• 141126-34-3 (Z)-1,2-bis-(benzylsulphonyl)ethylene 

Relevant academic research and scientific papers

The role of palladium catalyst and base in stereoselective transformations of (E)-2-chlorovinylsulfides

Stereoselective transformations of 2-chlorovinylsulfides in the presence of soluble (t-BuOK) or insoluble (solid KOH or Cs2CO 3/18-crown-6) base and palladium catalyst (dppb)Pd(OAc)2 have been studied. Depending on the sub

Synthesis of unsaturated organochalcogen compounds proceeding from dichloroethenes and organyl dichalcogenides

Reaction of 1,1- and 1,2-dichloroethenes with Ph2S2, Ph2Se2, Bn2S2, and i-Pr2S2 in a system hydrazine hydrate–KOH proceeds as a sequence of successive transformations: dehydrochlorination of initial dichloroethenes to form chloroacetylene, chlorine substitution for the chalcogen-containing nucleophile (ethynylchalcogenides formation), and the addition of the nucleophilic reagent to the triple bond affording 1,2- dichalcogenylethenes. In reactions with PhS– and PhSe? nucleophiles due to the high rate of all stages 1,2-bis (phenylchalcogenyl)ethenes are obtained having mainly the Z-configuration. In reactions with BnS? and i-PrS? in the IR, NMR and chromato-mass spectra intermediate ethynylchalcogenides were identified, and the final products consisted of a mixture with the prevalence of the Z-isomer.