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tert-butyl ethyl sulfoxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

25432-20-6

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25432-20-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 25432-20-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,4,3 and 2 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 25432-20:
(7*2)+(6*5)+(5*4)+(4*3)+(3*2)+(2*2)+(1*0)=86
86 % 10 = 6
So 25432-20-6 is a valid CAS Registry Number.

25432-20-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-ethylsulfinyl-2-methylpropane

1.2 Other means of identification

Product number -
Other names Aethyl-tert-butyl-sulfoxid

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:25432-20-6 SDS

25432-20-6Relevant academic research and scientific papers

Chemoselective α-sulfidation of amides using sulfoxide reagents

Leypold, Mario,D'Angelo, Kyan A.,Movassaghi, Mohammad

, p. 8802 - 8807 (2020/11/03)

The direct α-sulfidation of tertiary amides using sulfoxide reagents under electrophilic amide activation conditions is described. Employing convenient and readily available reagents, selective functionalization takes place to generate isolable sulfonium

A Convenient Procedure for the Oxidation of Sterically Hindered Sulfides to Sulfoxides

Drabowicz, Jozef,Lyzwa, Piotr,Popielarczyk, Miroslaw,Mikolajczyk, Marian

, p. 937 - 938 (2007/10/02)

A selective and efficient method for the oxidation of sterically hindered sulfides to sulfoxides is described, which involves the use of hydrogen peroxide in methanol in the presence of catalytic amounts of a mixture of sulfuric acid and isoamyl, isopropy

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