3070-15-3 Usage
Description
O,O-diethyl O-[4-(methylthio)phenyl] thiophosphate, also known as Fensulfothion Sulfide, is a metabolite derived from the insecticide fensulfonthion (F265490). It is characterized by its ability to inhibit cholinesterase activity, which plays a crucial role in the proper functioning of the nervous system.
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.
Check Digit Verification of cas no
The CAS Registry Mumber 3070-15-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,7 and 0 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3070-15:
(6*3)+(5*0)+(4*7)+(3*0)+(2*1)+(1*5)=53
53 % 10 = 3
So 3070-15-3 is a valid CAS Registry Number.
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
3070-15-3Relevant articles and documents
Photocatalytic Deoxygenation of Sulfoxides Using Visible Light: Mechanistic Investigations and Synthetic Applications
Clarke, Aimee K.,Parkin, Alison,Rossi-Ashton, James A.,Taylor, Richard J. K.,Unsworth, William P.
, p. 5814 - 5820 (2020/07/21)
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.
