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Benzene, [[2-(phenylmethoxy)ethyl]sulfonyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

122396-68-3

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122396-68-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 122396-68-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,3,9 and 6 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 122396-68:
(8*1)+(7*2)+(6*2)+(5*3)+(4*9)+(3*6)+(2*6)+(1*8)=123
123 % 10 = 3
So 122396-68-3 is a valid CAS Registry Number.

122396-68-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(benzenesulfonyl)ethoxymethylbenzene

1.2 Other means of identification

Product number -
Other names Benzene,[[2-(phenylmethoxy)ethyl]sulfonyl]

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:122396-68-3 SDS

122396-68-3Downstream Products

122396-68-3Relevant academic research and scientific papers

Radical induced allylations of functionalized α-haloalkylphenyl sulfones

Giardina, Alessandra,Giovannini, Riccardo,Petrini, Marino

, p. 1995 - 1998 (2007/10/03)

α-Haloalkylphenyl sulfones are efficiently allylated using allyltributyltin in benzene at reflux in the presence of AIBN. Several functional groups (e.g. eater, keto, amino, nitro etc.) are tolerated by these conditions that ultimately allow the chemoselective allylation of phenylsulfones at α position.

Microbial Asymmetric Oxidation of 2-Alkoxyethylsulfides and a Facile Synthesis of Chiral Vinyl Sulfoxide

Ohta, Hiromichi,Matsumoto, Shinsuke,Okamoto, Yasushi,Sugai, Takeshi

, p. 625 - 628 (2007/10/02)

2-Alkoxyethyl phenyl sulfides were oxidized by incubation with Rhodococcus equi IFO 3730 to afford chiral sulfoxides of high enantio excess.Phenyl vinyl sulfoxide and 2-hydroxyethyl phenyl sulfoxide were obtained from microbial oxidation products without any loss their optical purities.

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