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[2-(benzylsulfonyl)-1-chloroethyl]benzene is a chemical compound characterized by a benzene ring with a sulfonyl group and a chloroethyl group attached to it. The chemical structure consists of a benzene molecule with a benzylsulfonyl group and a chloroethyl group bonded to it, making it a versatile compound in organic synthesis and the development of new chemical entities.

30158-39-5

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30158-39-5 Usage

Uses

Used in Chemical Synthesis:
[2-(benzylsulfonyl)-1-chloroethyl]benzene is used as a reagent in various chemical reactions for the synthesis of different compounds. Its unique structure allows it to participate in a range of reactions, making it a valuable component in the creation of new molecules.
Used in Pharmaceutical Production:
In the pharmaceutical industry, [2-(benzylsulfonyl)-1-chloroethyl]benzene is used as an intermediate in the production of various drugs. Its properties enable it to be a key component in the development of new medications, potentially contributing to the treatment of various diseases and conditions.
Used in Agrochemical Development:
[2-(benzylsulfonyl)-1-chloroethyl]benzene also finds application in the agrochemical sector, where it is used as an intermediate for the synthesis of pesticides, herbicides, and other agricultural chemicals. Its role in this industry is crucial for the development of effective and environmentally friendly products to protect crops and enhance agricultural productivity.
Used in Industrial Product Manufacturing:
[2-(benzylsulfonyl)-1-chloroethyl]benzene's properties and uses extend to the manufacturing of various industrial products, where it serves as a building block for the creation of materials with specific characteristics. This makes [2-(benzylsulfonyl)-1-chloroethyl]benzene an important component in the development of innovative and high-performance materials for a wide range of applications.

Check Digit Verification of cas no

The CAS Registry Mumber 30158-39-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,1,5 and 8 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 30158-39:
(7*3)+(6*0)+(5*1)+(4*5)+(3*8)+(2*3)+(1*9)=85
85 % 10 = 5
So 30158-39-5 is a valid CAS Registry Number.

30158-39-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloro-2-phenylethyl 4-nitrophenyl sulfone

1.2 Other means of identification

Product number -
Other names 1-Chlor-1-phenyl-2-(p-nitrophenylsulfonyl)-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:30158-39-5 SDS

30158-39-5Relevant academic research and scientific papers

Cu-Catalyzed photoredox chlorosulfonation of alkenes and alkynes

Alkan-Zambada, Murat,Hu, Xile

, p. 4525 - 4533 (2019/04/25)

Visible-light photoredox chlorosulfonation of alkenes and alkynes is achieved using a Cu photocatalyst. The reactions occur under mild conditions, have broad scope, and have high functional group tolerance.

DESULFONYLATION OF ARYLMETHANESULFONYL CHLORIDES CATALYZED BY DICLHOROTRIS(TRIPHENYLPHOSPHINE)RUTHENIUM(II)

Kamigata, Nobumasa,Suzuki, Norihiro,Kobayashi, Michio

, p. 139 - 144 (2007/10/02)

Reactions of arylmethanesulfonyl chlorides catalyzed by dichlorotris(triphenylphosphine)ruthenium(II) (1) have been studied.Desulfonylation occurred when arylmethanesulfonyl chlorides were treated with catalytic amounts of the ruthenium(II) catalyst to give chloromethylarene in high yields.No addition of the sulfonyl chloride to olefin was observed when the reaction was carried out in the presence of an equimolar amount of an olefin such as styrene.However, the rate of disappearance of the sulfonyl chloride was accelerated by addition of an olefin.The desulfonylation is assumed to proceed by a redox transfer promoted homolytic mechanism in the coordination sphere of the catalyst.In the presence of large excess of styrenes, arylmethanesulfonyl chlorides added to the olefins to give 1:1 adducts competitively with the desulfonylation yielding chloromethylarenes.

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