25476-46-4 Usage
Uses
Used in Agricultural Applications:
Ethion is used as an insecticide and acaricide for controlling pests in various crops. It is applied to target a wide range of insects and mites that can cause significant damage to agricultural yields, thereby protecting the crops and increasing productivity.
Used in Horticultural Applications:
In horticulture, ethion serves a similar purpose as in agriculture, where it is used to manage pest populations that could otherwise harm ornamental plants, reducing their aesthetic value and marketability.
Used in Forestry Applications:
Ethion is also utilized in forestry to protect trees and other woody plants from pests, ensuring their health and contributing to the sustainability of forest ecosystems.
However, due to the environmental and health concerns associated with ethion, its use has been increasingly scrutinized, and there is a push towards adopting alternative, eco-friendly pest control measures.
Check Digit Verification of cas no
The CAS Registry Mumber 25476-46-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,4,7 and 6 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 25476-46:
(7*2)+(6*5)+(5*4)+(4*7)+(3*6)+(2*4)+(1*6)=124
124 % 10 = 4
So 25476-46-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H15O4PS2/c1-4-13(7)6-5-10-11(12,8-2)9-3/h4-6H2,1-3H3
25476-46-4Relevant academic research and scientific papers
Selective Sulfur Oxygenation in Phosphoroamidate, Thionophosphate, and Thiophosphate Agrochemicals by Perfluoro-cis-2,3-dialkyloxaziridine
Terreni, Marco,Pregnolato, Massimo,Resnati, Giuseppe,Benfenati, Emilio
, p. 7981 - 7992 (2007/10/02)
Several organophsophorus agrochemicals 2a-g with thioether, phosphoramidic, phosphorothioic, and phosphorothionic functions were reacted with perfluoro-cis-2-n-butyl-3-n-propyloxaziridine 1.The selective oxygenation of sulfide function to give sulfoxide derivatives 3a-g occured in high yields without overoxidation to sulfone products.Sulfoxides 3a-e were further oxidized under mild conditions to the corresponding sulfones 4a-e.All the products are themselves of interest as analytical environmental standards and their preparation is described in detail.
