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1001-62-3

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1001-62-3 Usage

General Description

Dimethanesulfonyl peroroxyde, also known as DPS, is a highly reactive and powerful oxidizing agent used in a variety of chemical reactions and industrial processes. It is characterized by its potential to release free radicals, making it an effective initiator for polymerization reactions. Additionally, DPS is commonly utilized in the synthesis of organic compounds, especially for the oxidation of sulfides to sulfoxides and for the cleavage of certain functional groups. However, it is important to handle this chemical with care due to its explosive nature and potential for causing severe skin and eye irritation. Furthermore, proper storage and handling procedures must be followed to ensure safety and prevent accidents in the workplace.

Check Digit Verification of cas no

The CAS Registry Mumber 1001-62-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,0 and 1 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1001-62:
(6*1)+(5*0)+(4*0)+(3*1)+(2*6)+(1*2)=23
23 % 10 = 3
So 1001-62-3 is a valid CAS Registry Number.
InChI:InChI=1/C2H6O6S2/c1-9(3,4)7-8-10(2,5)6/h1-2H3

1001-62-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name methylsulfonyloxy methanesulfonate

1.2 Other means of identification

Product number -
Other names -

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:1001-62-3 SDS

1001-62-3Relevant articles and documents

Late-Stage Aromatic C-H Oxygenation

B?rgel, Jonas,Tanwar, Lalita,Berger, Florian,Ritter, Tobias

, p. 16026 - 16031 (2018)

Synthetic methods for oxidative aromatic C-O bond formation are sparse, despite their demand in metabolite synthesis for drug discovery and development. We report a novel methodology for late-stage C-O bond formation of arenes. The reaction proceeds with excellent functional group tolerance even for highly functionalized substrates. The resulting aryl mesylates provide access to potential human metabolites of pharmaceuticals, and may be used directly to install a C-F bond to block metabolic hotspots. A charge-transfer interaction between the reagent bis(methanesulfonyl) peroxide and the substrate arenes may be relevant for the chemoselective functionalization of arenes over other functional groups.

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