3070-15-3

Usage

Uses

Used in Agricultural Industry:
O,O-diethyl O-[4-(methylthio)phenyl] thiophosphate is used as an insecticide for controlling a variety of pests in agricultural settings. Its application helps protect crops from damage caused by insects, ensuring a higher yield and better quality of produce.
Used in Environmental Protection:
In the field of environmental protection, O,O-diethyl O-[4-(methylthio)phenyl] thiophosphate is utilized to manage insect populations that can cause harm to ecosystems and natural habitats. By controlling these populations, it helps maintain a balance in the environment and prevents the spread of diseases that can be transmitted by insects.
Used in Public Health:
O,O-diethyl O-[4-(methylthio)phenyl] thiophosphate is also employed in public health initiatives to control insect-borne diseases. By targeting the insects that transmit diseases such as malaria, dengue, and Zika virus, it contributes to the reduction of disease transmission and improves overall public health.

InChI:InChI=1/C11H17O3PS2/c1-4-12-15(16,13-5-2)14-10-6-8-11(17-3)9-7-10/h6-9H,4-5H2,1-3H3

Upstream product

• 115-90-2 fensulfothion 
• 1073-72-9 4-hydroxythioanisole 
• 2524-04-1 diethyl phosphorochloridothioate 

Relevant academic research and scientific papers

Photocatalytic Deoxygenation of Sulfoxides Using Visible Light: Mechanistic Investigations and Synthetic Applications

The photocatalytic deoxygenation of sulfoxides to generate sulfides facilitated by either Ir[(dF(CF3)ppy)2(dtbbpy)]PF6 or fac-Ir(ppy)3 is reported. Mechanistic studies indicate that a radical chain mechanism operates, which proceeds via a phosphoranyl radical generated from a radical/polar crossover process. Initiation of the radical chain was found to proceed via two opposing photocatalytic quenching mechanisms, offering complementary reactivity. The mild nature of the radical deoxygenation process enables the reduction of a wide range of functionalized sulfoxides, including those containing acid-sensitive groups, in typically high isolated yields.

Reduction of CO2 with NaBH4/I2 for the Conversion of Thiophenols to Aryl Methyl Sulfides

We report a tandem reaction to realize reduction of carbon dioxide with thiophenols to generate aryl methyl sulfides under the NaBH4/I2 system with 18-crown-6 as the solvent. Thiophenols bearing electron-donating and electron-withdrawing groups are feasible in this reaction. Controlled experiment results indicate that 18-crown-6 plays a critical role in six-electron reduction of carbon dioxide.