24519-85-5 Usage
General Description
5,6-Dihydro-1,4-dithiin-2,3-dicarboximide is a chemical compound with the molecular formula C6H8N2O2S2. It is also known as malathion, which is commonly used as an insecticide to control pests in agriculture and public health. 5,6-DIHYDRO-1,4-DITHIIN-2,3-DICARBOXIMIDE works by inhibiting the activity of acetylcholinesterase, an enzyme that breaks down the neurotransmitter acetylcholine. By blocking this enzyme, malathion disrupts the normal function of the nervous system in insects, leading to paralysis and eventual death. However, it is important to note that malathion can also be toxic to humans and other non-target organisms, so it should be used with caution and according to safety guidelines.
Check Digit Verification of cas no
The CAS Registry Mumber 24519-85-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,5,1 and 9 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 24519-85:
(7*2)+(6*4)+(5*5)+(4*1)+(3*9)+(2*8)+(1*5)=115
115 % 10 = 5
So 24519-85-5 is a valid CAS Registry Number.
InChI:InChI=1/C6H5NO2S2/c8-5-3-4(6(9)7-5)11-2-1-10-3/h1-2H2,(H,7,8,9)
24519-85-5Relevant articles and documents
Biological evaluation of novel 1,4-dithiine derivatives as potential antimicrobial agents
Bielenica, Anna,Kossakowski, Jerzy,Struga, Marta,Dybala, Izabela,Colla, Paolo La,Tamburini, Elena,Loddo, Roberta
scheme or table, p. 1411 - 1420 (2012/06/04)
The preparation of twelve aminoalkanol derivatives of 2,3-dihydro-5H-[1,4] dithiino[2,3-c]pyrrole- 5,7(6H)-dione was described. Newly obtained compounds, as well as their propyl and butyl analogues, were evaluated in vitro against selected viruses. Select
Electronic effects in the acid-promoted deprotection of N-2,4-dimethoxybenzyl maleimides
Watson, Daniel J.,Dowdy, Eric D.,Li, Wen-Sen,Wang, Jianji,Polniaszek, Richard
, p. 1827 - 1830 (2007/10/03)
Cleavage of several 2,4-dimethoxybenzylmaleimides could be performed employing TFA in anisole. Electronic effects exemplified by varying the substitution present on the maleimide resulted in a variation in the rate of the deprotection. In contrast, 2,4-dimethoxybenzylsuccinimides were inert to the conditions.
