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2,3-DICHLOROPHENYLMETHYLSULFONE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

106418-92-2

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106418-92-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 106418-92-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,4,1 and 8 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 106418-92:
(8*1)+(7*0)+(6*6)+(5*4)+(4*1)+(3*8)+(2*9)+(1*2)=112
112 % 10 = 2
So 106418-92-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H6Cl2O2S/c1-12(10,11)6-4-2-3-5(8)7(6)9/h2-4H,1H3

106418-92-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-dichloro-3-methylsulfonylbenzene

1.2 Other means of identification

Product number -
Other names 2,3-dichlorophenyl methyl sulfone

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:106418-92-2 SDS

106418-92-2Downstream Products

106418-92-2Relevant academic research and scientific papers

Total Synergistic effect between triflic acid and bismuth(IIIr antimony(III) chlorides in catalysis of the Methanesulfonylation of Arenes

Peyronneau, Magali,Boisdon, Marie-Therese,Roques, Nicolas,Mazieres, Stephane,Le Roux, Christophe

, p. 4636 - 4640 (2007/10/03)

A total synergistic effect between bismuth(III) or antimony(III) chlorides and triflic acid has been observed in the Friedel-Crafts methanesulfonylation of arenes and has resulted in the development of the first efficient catalytic systems usable for the methanesulfonylation of both activated and deactivated arenes. A proposed mechanism to explain the observed effects is also discussed. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004.

An alternative synthesis of chlorinated biphenyl methylsulfonyl metabolites

Mortimer, Richard D.,Newsome, W. Harvey

, p. 935 - 946 (2007/10/03)

Published methods of synthesizing chlorinated biphenyl methylsulfones require the separation of a complex mixture of impurities and isomers using both normal and reverse phase HPLC. Even with semi-preparative scale equipment, the process is tedious and time-consuming. In this report, the palladium-catalyzed addition of an aryl iodide to an aryl trimethylstannane has been exploited to produce these compounds in high purity (≥ 99%) using conventional techniques of purification. The reaction has been demonstrated for a group of methylsulfonyl CBs representing 0 to 3 ortho-chlorine interactions between the biphenyl rings and with the methylsulfonyl group at either the 3- or 4- position.

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