41935-39-1 Usage
Uses
Used in Polymer Production:
Bis(2-phenoxyethyl) peroxydicarbonate is utilized as a radical initiator in the emulsion polymerization process, playing a crucial role in the production of polymers, resins, and adhesives. Its effectiveness in initiating the polymerization process makes it a valuable component in this industry.
Used in Specialty Chemical Synthesis:
bis(2-phenoxyethyl) peroxydicarbonate also finds application in the synthesis of specialty chemicals, where its strong oxidizing properties contribute to the formation of desired chemical products.
Used in Elastomer Production:
Furthermore, bis(2-phenoxyethyl) peroxydicarbonate serves as a crosslinking agent in the manufacturing of elastomers, enhancing their structural integrity and performance characteristics.
Check Digit Verification of cas no
The CAS Registry Mumber 41935-39-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,9,3 and 5 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 41935-39:
(7*4)+(6*1)+(5*9)+(4*3)+(3*5)+(2*3)+(1*9)=121
121 % 10 = 1
So 41935-39-1 is a valid CAS Registry Number.
InChI:InChI=1/C18H18O8/c19-17(23-13-11-21-15-7-3-1-4-8-15)25-26-18(20)24-14-12-22-16-9-5-2-6-10-16/h1-10H,11-14H2
41935-39-1Relevant academic research and scientific papers
Synthesis of peroxydicarbonates containing alkyl-aromatic fragments and investigation of their properties
Etlis, I.V.,Fomin, V.A.,Nozrina, F.D.
, p. 2010 - 2015 (2007/10/02)
The reaction of alkyl-substituted benzyl- and naphthylmethyl-chloroformates with Na2O2 or cyclohexyloxyperoxycarbonic acid at 0-5 deg C leads to symmetric and asymmetric peroxydicarbonates.Investigation of the thermolysis kinetics of the peroxides at 50-70 deg C showed that the structure of the organic fragment influences the rate of homolysis of the O-O bond to a great extent.This is characteristic in particular for compounds containing substituents in the ortho-position, where the presence of methyl radicals leads to a decrease in the contribution of the induced dissociation to the overall rate of homolysis of the peroxides obtained
