6552-21-2

Usage

Uses

Used in Agricultural Industry:
FENSULFOTHION-OXON is used as an insecticide for controlling a variety of pests that can cause significant damage to crops. Its application helps protect agricultural yields and ensures the quality of produce by reducing the impact of insect infestations.
Used in Public Health:
In the public health sector, FENSULFOTHION-OXON is utilized for vector control, particularly targeting insects that transmit diseases. By inhibiting the cholinesterase activity in these insects, it helps to reduce the spread of illnesses carried by mosquitoes, flies, and other disease vectors.
Used in Research:
FENSULFOTHION-OXON also serves as a valuable tool in scientific research, particularly in studies related to insect physiology, neurology, and the development of new pesticides. Understanding its mechanism of action can contribute to the advancement of pest control strategies and the creation of more effective and environmentally friendly insecticides.

InChI:InChI=1/C11H17O5PS/c1-4-14-17(12,15-5-2)16-10-6-8-11(9-7-10)18(3)13/h6-9H,4-5H2,1-3H3

Upstream product

• 42254-80-8 S-methyl thiosulfate O-sodium salt 

Relevant academic research and scientific papers

Aryl sulfoxide, thioether compound, synthesis method and application thereof

The invention discloses a method for selective synthesis of an aryl sulfoxide compound (III) and an aryl thioether compound (IV). According to the invention, in a reactive solvent, an aryl high iodinesalt is adopted as the reaction raw material, aryl/alkyl thiosulfate is taken as the vulcanizing reagent, under the catalysis of visible light and a photosensitive reagent, and under the action of lewis acid and alkali, when the reaction atmosphere is nitrogen, the thioether compound (IV) can be generated, and when the reaction atmosphere is air, the sulfoxide compound (III) can be generated. Thesynthesis method provided by the invention has the advantages of easily available and cheap raw materials, simple reaction operation, mild and environment-friendly reaction conditions, high yield, and excellent functional group tolerance. The invention also discloses the new aryl sulfoxide compound (III) and aryl thioether compound (IV), also successfully realizes later modification of drugs andsugar, and realizes the formal synthesis of some drugs, and provides an efficient method for selective construction of thioether and sulfoxide compounds.

Controllable Sulfoxidation and Sulfenylation with Organic Thiosulfate Salts via Dual Electron- and Energy-Transfer Photocatalysis

Sulfoxides and sulfides are two important functional groups in organic molecules, containing different valence states of sulfur. Both sulfoxidation and sulfenylation with common sulfurating reagents were successfully tuned via a facile variation of the atmosphere under photocatalyzed conditions. The sulfoxidation and sulfenylation transformations involved tandem electron-/energy-transfer and single-electron-transfer processes, respectively. Late-stage sulfoxidation for pharmaceuticals and sugar derivatives was established to be highly compatible. Divergent formal syntheses of sulfoxide/sulfide-containing marketed pharmaceuticals were switchably implemented. Gram-scale operations further demonstrated the practicability of the protocol.