241717
Phenyl vinyl sulfone
99%
Synonym(s):
(Ethenesulfonyl)benzene, (Ethenylsulfonyl)benzene, Ethenyl phenyl sulfone, Vinylsulfonylbenzene
Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Linear Formula:
C6H5SO2CH=CH2
CAS Number:
Molecular Weight:
168.21
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
226-890-2
Beilstein/REAXYS Number:
1906894
MDL number:
Assay:
99%
Form:
solid
InChI key
UJTPZISIAWDGFF-UHFFFAOYSA-N
InChI
1S/C8H8O2S/c1-2-11(9,10)8-6-4-3-5-7-8/h2-7H,1H2
SMILES string
C=CS(=O)(=O)c1ccccc1
assay
99%
form
solid
mp
67-69 °C (lit.)
solubility
organic solvents: soluble(lit.)
functional group
sulfone
Quality Level
Gene Information
human ... LOC129293(129293)
Related Categories
General description
Phenyl vinyl sulfone, a synthetic inhibitor of cysteine protease, exhibits antihelminthic and antiprotozoal properties.
Application
Phenyl vinyl sulfone was used as a common reagent in a variety of cycloaddition reactions to form cyclopropanes, cyclohexenes and cyclooctadienes.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Aldrichimica Acta, 15, 34-34 (1982)
Tetrahedron Letters, 34, 7583-7583 (1993)
Tetrahedron, 49, 5599-5599 (1993)
Tetrahedron, 49, 5495-5495 (1993)
Takuya Sueda et al.
Molecules (Basel, Switzerland), 10(1), 195-200 (2007-11-17)
Thermal decomposition of 1-tert-butylperoxy-1,2-benziodoxol-3(1H)-one in cyclic ethers and acetals at 50 degrees C generates alpha-oxy carbon-centered radicals, which undergo an addition reaction with vinyl sulfones and unsaturated esters.
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service