7594-45-8

Usage

Physical state

Colorless liquid

Odor

Strong and unpleasant

Usage

Starting material in the synthesis of organic compounds with thioether functional groups

Flammability

Flammable, should be handled with care

Storage

Cool, dry place and away from sources of ignition

Safety

Should be handled by trained professionals familiar with proper safety procedures.

Upstream product

• 14252-45-0 2,2-bis(ethylthio)propane 

Downstream Products

• 14252-45-0 2,2-bis(ethylthio)propane 
• 54410-62-7 1.2-Bis-(ethyl-mercapto)-propan 
• 142572-43-8 N-benzyl-3-ethylthio-1-phenyl-3-butenylamine 
• 74-85-1 ethene 

Relevant academic research and scientific papers

Structure-Stability Relationships in Vinyl Sulfides. I. On the Stable Conformations of Vinyl Sulfides

A thermodynamic and 13C NMR spectroscopic study of the structures of the less stable rotamers of alkyl vinyl sulfides have been performed.It has been shown that the less stable rotamer of methyl vinyl sulfide has the planar s-trans configuration and the proportion of this is about 20percent.The energy difference between the planar s-cis and s-trans is about 3.5 kJ mol-1.Ethyl vinyl sulfide is almost an equimolar mixture of the planar s-cis and s-trans conformations.The 13C NMR data showed that the p-? cojugation in the compounds that could not adopt any of the planar arrangements was decreased.In alkyl 1-propenyl sulfides, the stabilizing interaction between the methyl group and the S atom cis to each other was ca.1.8 kJ mol-1.The most probable choice for the most stable conformation of di-1-propenyl sulfides is the planar (or nearly planar) s-trans,s-trans one.