Skip to Content
Merck
All Photos(1)

Key Documents

241717

Sigma-Aldrich

Phenyl vinyl sulfone

99%

Synonym(s):

(Ethenesulfonyl)benzene, (Ethenylsulfonyl)benzene, Ethenyl phenyl sulfone, Vinylsulfonylbenzene

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
C6H5SO2CH=CH2
CAS Number:
Molecular Weight:
168.21
Beilstein:
1906894
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

99%

form

solid

mp

67-69 °C (lit.)

solubility

organic solvents: soluble(lit.)

functional group

sulfone

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

Looking for similar products? Visit Product Comparison Guide

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 Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Tetrahedron, 49, 5495-5495 (1993)
Aldrichimica Acta, 15, 34-34 (1982)
Tetrahedron Letters, 34, 7583-7583 (1993)
Yumiko Nakayama et al.
Environmental sciences : an international journal of environmental physiology and toxicology, 12(6), 371-379 (2006-04-13)
To investigate the safe handling of an industrial product, phenyl vinyl sulfone (PVS), which has an extremely high potential for dermal sensitization at low concentrations and positive mutagenicity, the maximum no-effect concentration for dermal deposits was obtained from dermal sensitization
Catalytic enantioselective reduction of beta,beta-disubstituted vinyl phenyl sulfones by using bisphosphine monoxide ligands.
Jean-Nicolas Desrosiers et al.
Angewandte Chemie (International ed. in English), 46(31), 5955-5957 (2007-06-07)

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