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Benzene, (2-butenylsulfinyl)-, (E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

86838-05-3

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86838-05-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86838-05-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,8,3 and 8 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 86838-05:
(7*8)+(6*6)+(5*8)+(4*3)+(3*8)+(2*0)+(1*5)=173
173 % 10 = 3
So 86838-05-3 is a valid CAS Registry Number.

86838-05-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name γ-methylallyl phenyl sulphoxide

1.2 Other means of identification

Product number -
Other names (but-2t-ene-1-sulfinyl)-benzene

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:86838-05-3 SDS

86838-05-3Relevant academic research and scientific papers

TELLURIUM DIOXIDE CATALYZED SELECTIVE OXIDATION OF SULFIDES TO SULFOXIDES WITH HYDROGEN PEROXIDE

Kim, Kwan Soo,Hwang, Hye Jung,Cheong, Chan Seong,Hahn, Chi Sun

, p. 2893 - 2894 (2007/10/02)

TeO2-H2O2 system was found to be an efficient selective reagent for the oxidation of sulfides to sulfoxides in the presence of other common functional groups.Over-oxidation of sulfoxides to sulfones was not observed.

Asymmetric Induction in the Additions of Anions of Allylic Sulfoxides to Benzaldehyde

Antonjuk, David J.,Ridley, Damon D.,Smal, Mary A.

, p. 2635 - 2651 (2007/10/02)

Addition reactions of anions of aryl allyl sulfoxides to benzaldehyde proceed readily in moderate yields and afford mixtures of products resulting from α- and γ-attack on the allyl anion.The γ-products all possess the (E)-configuration around the double bond, and asymmetric induction occurs in the addition to the extent that the major/minor diastereomer ratio exceeds 2:1, generally.Electronic factors are believed to be responsible for this "remote" asymmetric induction.Mixtures of all four possible diastereomers are observed in the products from α-attack and evidence is presented which suggests that the ratios of these products are as a result of epimerization of two of the chiral centres by sigmatropic rearrangement.

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