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disulfoton-oxon-sulfoxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

2496-92-6

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2496-92-6 Usage

Chemical Properties

Pale Yellow Oil

Check Digit Verification of cas no

The CAS Registry Mumber 2496-92-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,9 and 6 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2496-92:
(6*2)+(5*4)+(4*9)+(3*6)+(2*9)+(1*2)=106
106 % 10 = 6
So 2496-92-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H19O4PS2/c1-4-11-13(9,12-5-2)14-7-8-15(10)6-3/h4-8H2,1-3H3

2496-92-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-diethoxyphosphorylsulfanyl-2-ethylsulfinylethane

1.2 Other means of identification

Product number -
Other names Thiol systox sulfoxide

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:2496-92-6 SDS

2496-92-6Downstream Products

2496-92-6Relevant academic research and scientific papers

Selective Sulfur Oxygenation in Phosphoroamidate, Thionophosphate, and Thiophosphate Agrochemicals by Perfluoro-cis-2,3-dialkyloxaziridine

Terreni, Marco,Pregnolato, Massimo,Resnati, Giuseppe,Benfenati, Emilio

, p. 7981 - 7992 (2007/10/02)

Several organophsophorus agrochemicals 2a-g with thioether, phosphoramidic, phosphorothioic, and phosphorothionic functions were reacted with perfluoro-cis-2-n-butyl-3-n-propyloxaziridine 1.The selective oxygenation of sulfide function to give sulfoxide derivatives 3a-g occured in high yields without overoxidation to sulfone products.Sulfoxides 3a-e were further oxidized under mild conditions to the corresponding sulfones 4a-e.All the products are themselves of interest as analytical environmental standards and their preparation is described in detail.

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