35444-20-3 Usage
Uses
Used in Organic Synthesis:
Potassium ethyl trithiocarbonate is used as an intermediate in the production of dithiocarbamate derivatives, which are employed as fungicides, bactericides, and herbicides. Its ability to form stable complexes with various metals makes it a valuable tool in inorganic chemistry and metallurgy.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, potassium ethyl trithiocarbonate is used as a reagent in the synthesis of certain pharmaceuticals, contributing to the development of new drugs and therapeutic agents.
Used in Rubber Production:
As a vulcanization accelerator, potassium ethyl trithiocarbonate is utilized in the production of rubber, enhancing the process and improving the properties of the final rubber products.
Safety Precautions:
It is important to handle potassium ethyl trithiocarbonate with care, as it is a potential irritant to the eyes and skin and may be harmful if ingested or inhaled. Proper safety measures should be taken during its use to minimize any risks associated with its handling and application.
Check Digit Verification of cas no
The CAS Registry Mumber 35444-20-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,4,4 and 4 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 35444-20:
(7*3)+(6*5)+(5*4)+(4*4)+(3*4)+(2*2)+(1*0)=103
103 % 10 = 3
So 35444-20-3 is a valid CAS Registry Number.
InChI:InChI=1/C3H6S3.K.H/c1-2-6-3(4)5;;/h2H2,1H3,(H,4,5);;/q;+1;-1
35444-20-3Relevant academic research and scientific papers
Thioacid radical terminated mercaptosilane coupling agent, synthesis method and applications thereof
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Paragraph 0067-0068; 0070, (2020/06/02)
The invention belongs to a silane coupling agent, and particularly relates to a thioacid radical-terminated mercaptosilane coupling agent, a synthesis method and applications thereof, wherein the thioacid radical-terminated mercaptosilane coupling agent has a structure represented by a formula (I). According to the thioacid radical-terminated mercaptosilane coupling agent represented by the formula (I), the interaction between a polymer and a filler can be enhanced, the hysteresis loss of a rubber material is reduced, the Payne effect of the rubber material is reduced, and the dispersity of white carbon black is improved, so that the oil consumption and the emission of carbon dioxide in a tire driving process are reduced, and the wear resistance of the tire is enhanced.
Synthesis and Physical Properties of First 5,5'-Bridged Bis(1,3-dithiolylium-4-olates)
Gotthardt, Hans,Pflaumbaum, Wolfgang
, p. 411 - 420 (2007/10/02)
The synthesis and spectroscopic properties of the novel title compounds of type 6 and 17, which contain two identical mesoionic systems linked together at the 5-positions, as well as the polymerization to 18 and the dimerization of 6c-e to 20a-c are described.
