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87157-78-6

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87157-78-6 Usage

Description

[2-(Ethenylsulfonyl)ethyl]benzene, commonly known as styrene sulfone, is an organic compound characterized by the molecular formula C10H12O2S. It features a benzene ring with a sulfone group and an ethenyl group attached, showcasing its unique chemical structure and properties.

Uses

Used in Polymer Production:
[2-(Ethenylsulfonyl)ethyl]benzene is utilized as a key component in the manufacturing of various polymers, such as polystyrene and resins. Its chemical structure contributes to the formation and properties of these polymers, making it an essential material in this application.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, [2-(ethenylsulfonyl)ethyl]benzene finds its use in the development and synthesis of different medicinal compounds. Its unique chemical properties allow it to be a valuable intermediate in the production of pharmaceuticals.
Used in Agricultural Chemicals:
[2-(ethenylsulfonyl)ethyl]benzene also plays a role in the agricultural chemicals industry, where it is employed in the creation of various agrochemical products. Its contribution to the development of these chemicals aids in enhancing agricultural productivity and crop protection.
Safety Precautions:
It is crucial to note that [2-(ethenylsulfonyl)ethyl]benzene is considered toxic and can cause irritation to the skin, eyes, and respiratory system. Prolonged exposure may result in liver and kidney damage. Therefore, it is essential to handle and store this chemical compound with care, adhering to safety guidelines and regulations for its use.

Check Digit Verification of cas no

The CAS Registry Mumber 87157-78-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,1,5 and 7 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 87157-78:
(7*8)+(6*7)+(5*1)+(4*5)+(3*7)+(2*7)+(1*8)=166
166 % 10 = 6
So 87157-78-6 is a valid CAS Registry Number.

87157-78-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-ethenylsulfonylethylbenzene

1.2 Other means of identification

Product number -
Other names 2-Vinylsulfon-1-phenyl-aethan

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:87157-78-6 SDS

87157-78-6Downstream Products

87157-78-6Relevant articles and documents

The epoxy-Ramberg-Baecklund reaction (ERBR): A sulfone-based method for the synthesis of allylic alcohols

Evans, Paul,Johnson, Paul,Taylor, Richard J. K.

, p. 1740 - 1754 (2007/10/03)

The epoxy-Ramberg-Baecklund reaction (ERBR) is outlined, in which α,β-epoxy sulfones are converted into a range of mono-, di- and tri-substituted allylic alcohols, on treatment with base. Modification of this method enabled the preparation of enantio-enriched allylic alcohols following the diastereoselective epoxidation of enantio-enriched vinyl sulfones that were accessed efficiently from the chiral pool. The scope, optimisation and limitations of the ERBR as a method for the preparation of allylic alcohols are discussed. Wiley-VCH Verlag GmbH & Co. KGaA, 2006.

New ω-phthalimidoperoxyalkanoic acids in decontamination. Destruction of some toxic organophosphorus and organosulfur pollutants

Lion,Da Conceicao,Delmas,Magnaud

, p. 1182 - 1184 (2007/10/03)

Chemical decontamination of toxic compounds (chemical warfare agents and/or insecticides) is of increasing importance. In this study, we report the use of ω-phthalimidoperoxyalkanoic acids 2 in the destruction of paraoxon (O,O-diethyl-O-para-nitrophenylphosphate), a well-known insecticide, and 2-chloro-2′-phenyldiethyl sulfide (a half mustard). We show that while all the peroxyacids used in this series allow the destruction of toxic compounds, the length n of the alkanoic side chain is important to the choice of the optimal industrial compound, which is 2d (n = 5).

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