3559-73-7 Usage
Uses
Used in Pesticide Industry:
Dicofol is used as a pesticide and acaricide for controlling pests and mites in agricultural settings. Its application is aimed at protecting crops from damage caused by these organisms, thereby ensuring a higher yield and better quality of produce.
Used in Acaricide Applications:
In the field of acaricides, Dicofol is utilized to combat mite infestations, which can be detrimental to both agricultural crops and the health of humans and animals. Its effectiveness in targeting acetylcholinesterase makes it a valuable tool in managing mite populations.
However, it is important to note that due to potential health and environmental risks associated with Dicofol, its use has been restricted or banned in several countries. Exposure to Dicofol has been linked to various health effects, such as skin and eye irritation, respiratory issues, and potential carcinogenicity. Therefore, its application and handling should be done with caution and in adherence to strict safety guidelines to minimize the risks to human health and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 3559-73-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,5 and 9 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3559-73:
(6*3)+(5*5)+(4*5)+(3*9)+(2*7)+(1*3)=107
107 % 10 = 7
So 3559-73-7 is a valid CAS Registry Number.
3559-73-7Relevant academic research and scientific papers
SYNTHESES AND REACTIONS OF PHENYLTHIO AND PROPYLTHIOACETYLENIC COMPOUNDS
Nagashima, Enkou,Suzuki, Kunio,Sekiya, Minoru
, p. 1274 - 1279 (2007/10/02)
Reactions of 2,2-dichlorovinyl sulfides and their sulfoxide and sulfone derivatives with tert-butoxide and with organolithium compounds have provided entries to chloroethynyl sulides, tert-butoxyethynyl sulfides and their derivatives.Application of these reactions for the synthesis of several functional derivatives is also described.Keywords: 2,2-dichlorovinyl sulfide; chloroethynyl sulfide; tert-butoxyethynyl sulfide; ethynyl sulfide; cyclobutenone
FREE-RADICAL CHLOROVINYLATION OF AROMATIC AND ALIPHATIC THIOLS
Mirskova, A. N.,Martynov, A. V.,Voronkov, M. G.
, p. 1766 - 1773 (2007/10/02)
During the free-radical thiylation of trichloroethylene with organic thiols β,β-dichlorovinyl sulfides are formed in a single stage.The reaction of alkanethiols with tetrachloroethylene under analogous conditions leads to trichlorovinyl sulfides.Oxidation of β,β-dichlorovinyl sulfides with hydrogen peroxide in acetic acid leads to the corresponding β,β-dichlorovinyl sulfones.
