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About This Item
Linear Formula:
C6H5SO2CH=CH2
CAS Number:
Molecular Weight:
168.21
EC Number:
226-890-2
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
1906894
MDL number:
grade
purum
assay
≥98.0% (GC)
mp
67-69 °C (lit.), 68-70 °C
SMILES string
C=CS(=O)(=O)c1ccccc1
InChI
1S/C8H8O2S/c1-2-11(9,10)8-6-4-3-5-7-8/h2-7H,1H2
InChI key
UJTPZISIAWDGFF-UHFFFAOYSA-N
Gene Information
human ... LOC129293(129293)
Other Notes
Dienophile; adducts can conveniently be transformed into alkanes or ketones (equivalent of ethylene or ketene), review
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
Regulatory Information
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Moshira M F Helmy et al.
Experimental parasitology, 119(1), 125-134 (2008-02-23)
Phenyl vinyl sulfone is a synthetic inhibitor of cysteine protease and has antihelminthic and antiprotozoal properties. Phenyl vinyl sulfone was assayed in vitro for antifasciola activity against adult Fasciola gigantica worms using a well-established culture medium. Worms were treated with
M Varenberg et al.
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To analyse the performance of mushroom-shaped fibrillar adhesive microstructure, its behaviour was studied during different stages of attachment-loading-detachment cycle. Visualizing the evolutions of real contact area of single microfibres, it is shown that the mushroom-shaped geometry of contact elements promotes
Eric T Larson et al.
The Journal of biological chemistry, 284(39), 26839-26850 (2009-07-15)
The protozoan parasite Toxoplasma gondii relies on post-translational modification, including proteolysis, of proteins required for recognition and invasion of host cells. We have characterized the T. gondii cysteine protease cathepsin L (TgCPL), one of five cathepsins found in the T.
Sijiu Liu et al.
Journal of the American Chemical Society, 130(26), 8251-8260 (2008-06-06)
Protein tyrosine phosphatases (PTPs) play key roles in the regulation of normal and pathological processes ranging from cell proliferation, differentiation, metabolism, and survival to many human diseases including cancer and diabetes. Functional studies of PTP can be greatly facilitated by
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.
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