Welcome to LookChem.com Sign In|Join Free
  • or
5,6-Dihydro-1,4-dithiin-2,3-dicarboximide, commonly known as malathion, is a chemical compound with the molecular formula C6H8N2O2S2. It is an organophosphate insecticide that is widely used in agriculture and public health for pest control. Malathion operates by inhibiting the activity of acetylcholinesterase, an enzyme crucial for the breakdown of the neurotransmitter acetylcholine, thereby disrupting the nervous system function in insects and causing paralysis and death.

24519-85-5

Post Buying Request

24519-85-5 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

24519-85-5 Usage

Uses

Used in Agricultural Applications:
5,6-Dihydro-1,4-dithiin-2,3-dicarboximide is used as an insecticide in agriculture for controlling a variety of pests that can damage crops and reduce yields. Its application helps protect crops from insects such as aphids, mites, and mosquitoes, ensuring a more abundant and stable food supply.
Used in Public Health Applications:
In public health, 5,6-dihydro-1,4-dithiin-2,3-dicarboximide is utilized for controlling disease-transmitting insects, such as mosquitoes that spread malaria, dengue, and other vector-borne diseases. By reducing the population of these insects, the spread of diseases can be minimized, contributing to improved public health.
Used in Veterinary Medicine:
5,6-Dihydro-1,4-dithiin-2,3-dicarboximide is also used in veterinary medicine to control pests in livestock and poultry. It helps protect animals from infestations that can cause stress, reduce productivity, and spread diseases.
Used in Household Pest Control:
Malathion is used in household pest control products to manage insects that can infest homes, such as cockroaches and flies. Its application helps maintain a clean and healthy living environment by reducing the presence of these pests.

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)

24519-85-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-dihydro-[1,4]dithiino[2,3-c]pyrrole-5,7-dione

1.2 Other means of identification

Product number -
Other names 5,6-Dihydro-1,4-dithiin-2,3-dicarboximide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:24519-85-5 SDS

24519-85-5Relevant academic research and scientific papers

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

Pyrazine-2,3-dicarbonitriles substituted with maleimide derivatives

Morkved

, p. 1197 - 1201 (2008/09/19)

Syntheses and spectroscopic characteristics are reported for eight pyrazine-2,3-dicarbonitriles substituted with maleimide residue in addition to phenyl, 2-thienyl, or 2-furyl substituent.

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.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 24519-85-5