32341-86-9 Usage
Uses
Used in Plastics and Rubber Industry:
[bis(ethylsulfonyl)methyl]benzene is used as a crosslinking agent for enhancing the structural integrity and durability of plastics and rubbers. Its incorporation into these materials leads to improved mechanical properties and resistance to various environmental factors.
Used in Pharmaceutical Synthesis:
As a chemical intermediate, [bis(ethylsulfonyl)methyl]benzene plays a crucial role in the synthesis of various pharmaceuticals and organic compounds. Its unique chemical structure allows for the development of new drugs and medications that can address a wide range of health conditions.
Used in Industrial Processes:
[bis(ethylsulfonyl)methyl]benzene is also utilized as a solvent and a surfactant in different industrial processes. Its solvent properties enable it to dissolve a variety of substances, making it a valuable component in the production of various products. Additionally, its surfactant characteristics contribute to the stabilization and emulsification of mixtures in numerous applications.
Safety Precautions:
Given its classification as a hazardous chemical, [bis(ethylsulfonyl)methyl]benzene should be handled with care to prevent skin and eye irritation. It is also essential to avoid ingestion or inhalation, as these can lead to harmful health effects. Proper safety measures and handling protocols should be followed to minimize the risks associated with [bis(ethylsulfonyl)methyl]benzene.
Check Digit Verification of cas no
The CAS Registry Mumber 32341-86-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,3,4 and 1 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 32341-86:
(7*3)+(6*2)+(5*3)+(4*4)+(3*1)+(2*8)+(1*6)=89
89 % 10 = 9
So 32341-86-9 is a valid CAS Registry Number.
32341-86-9Relevant academic research and scientific papers
Proton Transfer from Carbon. A Study of the Acid-Base-catalysed Relaxation and the Bromination of Aryl-substituted Methanedisulfones
Aiken, Fiona,Cox, Brian G.,Soerensen, Poul E.
, p. 783 - 790 (2007/10/02)
Seven aryl-substituted derivatives of bis(ethylsulfonyl)methane have been synthesized and studied thermodynamically and kinetically in aqueous solution with respect to proton abstraction from the central carbon atom.The acidities of the six carbon acids are in the range pKA 10-12.The relaxation times of the reactions were studied by a spectrophotometric temperature-jump technique (hydroxide ion and phenolates as proton acceptors) and are in the microsecond range.The rates of bromination of the various carbanions have also been studied (potentiometrically) and the reactions are shown to be almost diffusion-controlled, with no marked trend with aromatic substituent.A small chemical activation may be due to a steric effect by the two sulfonyl groups.The rates of deprotonation, however, show considerable chemical activation, i.e., intrinsic rates are 3-4 orders of magnitude lower than for normal acids, indicating partial delocalization of the negative charge on the carbanion.This effect is somewhat larger than for cyano-activated carbon acids but considerably smaller than for carbon acids activated by carbonyl or nitro groups.It is concluded that sulfonyl groups interact with carbanions primarily by polar effects, but also, to some extent, mesomerically.The degree of mesomerism is, however, uncertain because part of the intrinsic barrier may derive from steric effects, as is also observed for bromination.
