| Weight | 168.217 g/mol |
|---|---|
| Formula | C8H8O2S |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 2 |
Phenyl vinyl sulfone (5535-48-8)
PVS cpd
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- Dienophilic properties of phenyl vinyl sulfone and trans-1-(phenylsulfonyl)-2-(trimethylsilyl)ethylene. Their utilization as synthons for ethylene, 1-alkenes, acetylene, and monosubstituted alkynes in the construction of functionalized six-membered rings via [4 + 2] .pi. cycloaddition methodology (Journal of Organic Chemistry, 1983)
- An ethylene and terminal olefin equivalent in [4 + 2] .pi. cycloadditions. General synthetic application of phenyl vinyl sulfone to the construction of functionalized six-membered rings (Journal of the American Chemical Society, 1980)
- Oxidative desulfonylation. Phenyl vinyl sulfone as a ketene synthetic equivalent (Tetrahedron Letters, 1980)
- Silver Acetate/TFBiphamPhosCatalyzed endoSelective Enantioselective 1,3Dipolar Cycloaddition of Azomethine Ylides with Vinyl Phenyl Sulfone (Advanced Synthesis & Catalysis, 2009)
- Copolymerization Characteristics and Spectra of Phenyl Vinyl Sulfide and Sulfone (Journal of the American Chemical Society, 1953)
- Toxoplasma gondii Cathepsin L Is the Primary Target of the Invasion-inhibitory Compound Morpholinurea-leucyl-homophenyl-vinyl Sulfone Phenyl (Journal of Biological Chemistry, 2009)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - PVS cpd
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SMILESC=CS(=O)(=O)C1=CC=CC=C1
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InChIKeyUJTPZISIAWDGFF-UHFFFAOYSA-N
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Phenyl vinyl sulfone
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