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7484-34-6

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7484-34-6 Usage

General Description

2,2'-(Ethylenebissulfonyl)diethanol is a chemical compound used primarily as a reactive intermediate in the production of polymers, surfactants, and pharmaceuticals. It is a dichlorosulfonyl compound that is highly reactive and is often used in the synthesis of complex organic molecules. 2,2'-(Ethylenebissulfonyl)diethanol is also used as a cross-linking agent in the manufacturing of polymers and resins. Due to its versatile chemical properties, 2,2'-(Ethylenebissulfonyl)diethanol has a wide range of applications in various industries, including plastics, textiles, and pharmaceuticals. However, it is important to handle this compound with caution as it can be hazardous if not handled properly.

Check Digit Verification of cas no

The CAS Registry Mumber 7484-34-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,8 and 4 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7484-34:
(6*7)+(5*4)+(4*8)+(3*4)+(2*3)+(1*4)=116
116 % 10 = 6
So 7484-34-6 is a valid CAS Registry Number.

7484-34-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[2-(2-hydroxyethylsulfonyl)ethylsulfonyl]ethanol

1.2 Other means of identification

Product number -
Other names 3,6-dithiaoctane-1,8-diol

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:7484-34-6 SDS

7484-34-6Downstream Products

7484-34-6Relevant articles and documents

Solvent-free chemoselective oxidation of thioethers and thiophenes by mechanical milling

Cravotto, Giancarlo,Garella, Davide,Carnaroglio, Diego,Gaudino, Emanuela Calcio,Rosati, Ornelio

, p. 11632 - 11634,3 (2012/12/12)

Organosulphur compounds can be easily and selectively oxidized to sulfones using a small excess of Oxone (1.6 eq.) under solventless mechanical milling conditions. This green procedure has been efficiently applied to a series of model compounds and to the desulphurization of medium/high sulphur content paraffins (up to 3000 mg kg-1).

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