7484-34-6 Usage
Uses
Used in Polymer Production:
2,2'-(Ethylenebissulfonyl)diethanol is used as a reactive intermediate for the synthesis of polymers, contributing to the formation of complex organic molecules that enhance the properties of the final polymer products.
Used in Surfactant Production:
In the surfactant industry, 2,2'-(Ethylenebissulfonyl)diethanol is utilized as a reactive intermediate, playing a crucial role in the creation of surfactants that have specific properties for various applications, such as detergents and emulsifiers.
Used in Pharmaceutical Industry:
2,2'-(Ethylenebissulfonyl)diethanol is employed as a reactive intermediate in the pharmaceutical sector, aiding in the development of new drugs and improving the synthesis of existing pharmaceutical compounds.
Used as a Cross-linking Agent:
2,2'-(Ethylenebissulfonyl)diethanol is used as a cross-linking agent in the manufacturing of polymers and resins, enhancing their structural integrity and performance characteristics.
Used in Textile Industry:
In the textile industry, 2,2'-(Ethylenebissulfonyl)diethanol is used as a reactive intermediate for the production of specialty fibers and fabrics, improving their durability and functionality.
Used in Plastics Industry:
2,2'-(Ethylenebissulfonyl)diethanol is utilized in the plastics industry as a reactive intermediate, contributing to the development of advanced plastic materials with improved properties for various applications.
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.
7484-34-6Relevant academic research and scientific papers
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).
Hydrolysis and oxidation products of the chemical warfare agents 1,2-Bis[(2-chloroethyl)thio]ethane Q and 2,2′-Bis(2-chloroethylthio) diethyl ether T
Timperley, Christopher M.,Black, Robin M.,Bird, Michael,Holden, Ian,Mundy, Joanna L.,Read, Robert W.
, p. 2027 - 2046 (2007/10/03)
Syntheses of diols of structure [HOCH2CH2S] 2(CH2)n in 86-95% yield from the sodium salt of 2-mercaptoethanol and Br(CH2)nBr (n = 1 to 5) or in 60-90% yield from 2-chloroethanol and NaS(CH2)nSNa (n = 2 to 5) are described. The diol [HOCH2CH2SCH 2CH2]2O was prepared in 82% yield from the sodium salt of 2-mercaptoethanol and [ClCH2CH2] 2O, and in 88% yield from 2-chloroethanol and [HSCH 2CH2]2O. Mono- and bis-sulfoxides and bis-sulfones of these species were prepared in generally high yield by treatment with an equivalent of KIO4 in aqueous methanol, two equivalents of NaIO4 in aqueous methanol, or four equivalents of H2O2 in trifluoroacetic acid respectively. The compounds are important analytical standards for investigating the fate of the chemical warfare agents sesquimustard Q and oxygen mustard T in environmental samples.
