63009-98-3 Usage
Description
[1,2,8]Thiadiazocane 1,1-dioxide, also known as Thimonacic acid, is a heterocyclic chemical compound with the molecular formula C2H4N2O2S. It features a seven-membered ring structure containing three nitrogen atoms, one sulfur atom, and two oxygen atoms. Thimonacic acid is recognized for its low toxicity to mammals and high efficacy in controlling pests and pathogens, making it a valuable component in integrated pest management strategies.
Uses
Used in Agricultural Applications:
[1,2,8]Thiadiazocane 1,1-dioxide is used as a pesticide and fungicide for controlling the development of insects and fungi in crops. Its application reason is due to its high efficacy in managing pests and pathogens, while maintaining low toxicity to mammals, which helps in preserving the ecological balance and ensuring the safety of the environment and human health.
Used in Integrated Pest Management Strategies:
[1,2,8]Thiadiazocane 1,1-dioxide is used as a key component in integrated pest management strategies for its ability to regulate the growth of insects and fungi, thus contributing to the overall effectiveness of these strategies in maintaining agricultural productivity and sustainability.
Check Digit Verification of cas no
The CAS Registry Mumber 63009-98-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,0,0 and 9 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 63009-98:
(7*6)+(6*3)+(5*0)+(4*0)+(3*9)+(2*9)+(1*8)=113
113 % 10 = 3
So 63009-98-3 is a valid CAS Registry Number.
63009-98-3Relevant articles and documents
Microwave-assisted synthesis of some substituted sulfamides
Gediz Erturk, Aliye,Bekdemir, Yunus
, p. 285 - 292 (2014/01/06)
Microwave-assisted synthesis of some substituted open-chain and cyclic sulfamides, by amine-exchange reaction, was studied in a modified domestic microwave oven. Reaction times and yields under microwave radiation were compared with classical heating. Synthesis of the sulfamides under microwave irradiation gave better yields with the desired compounds, and in considerably reduced reaction times, than those obtained by classical heating. [Supplementary materials are available for this article. Go to the publisher's online edition of Phosphorus, Sulfer, and Silicon and the Related Elements for the following free supplemental files: Additional figures.]
