6278-47-3

Usage

Uses

Used in Agricultural Industry:
Phosphonothioicdiamide, N,N'-diethyl-P-phenyl(6CI,8CI,9CI) is used as an insecticide and acaricide for controlling a wide range of pests, including aphids, thrips, and mites, in agricultural settings. It functions by inhibiting the activity of the enzyme acetylcholinesterase, leading to the accumulation of acetylcholine in the nervous system of the targeted pests, which results in their paralysis and death.
Used in Veterinary Products:
Phosphonothioicdiamide, N,N'-diethyl-P-phenyl(6CI,8CI,9CI) is also used in some veterinary products for controlling parasites in livestock. It has low toxicity to mammals, making it suitable for this application.
Environmental Considerations:
It is important to use Phosphonothioicdiamide, N,N'-diethyl-P-phenyl(6CI,8CI,9CI) with caution due to its potential toxicity to aquatic organisms. Proper handling and application methods should be employed to minimize its environmental impact.

Upstream product

• 75-04-7 ethylamine 
• 3497-00-5 phenylthiophosphonic acid dichloride 

Relevant academic research and scientific papers

Phosphorus-nitrogen compounds. Part 56. The solution synthesis of some trans-1,3-dialkyl-2,4-diphenyl-2,4-dithiocyclodi-λ5- phosphazanes and their proton, carbon-13, and phosphorus-31 nuclear magnetic resonance spectra

A series of trans-1,3-dialkyl-2,4-diphenyl-2,4-dithiocyclodi- λ5-phosphazanes, [PhP(S)NR]2 (R = Me, Et, Pr n, Pri, Bun, Bui, Bus, But, neopentyl, CH2Ph, or cyclohexyl) has been synthesized by a solution method and their proton, carbon-13, and phosphorus-31 n.m.r. spectra obtained. The relationships between phosphorus-31 and carbon-13 n.m.r. chemical shift data are explored; interpretation of proton n.m.r. data has led to the assignment of trans structures for the cyclodi-λ5- phosphazane molecules. Inductive and resonance substituent coefficients have been evaluated using the dual-substituent parameter method from the relative shieldings of the meta- and para-carbon nuclei in the phenyl ring.

Phosphorus-Nitrogen Compounds. Part 51. Carbon-13 and Phosphorus-31 Nuclear Magnetic Resonance Properties of Phenylphosphonothioic Di(monoalkylamides). Determination of Aromatic Substituent Constants by (13)C Nuclear Magnetic Resonance Spectroscopy

Carbon-13 and phosphorus-31 n.m.r. spectra have been obtained for a series of phenyl-phosphonothioic di(monoalkylamides), PhP(S)(NHR)2 (R=H, Me, Et, Prn, Pri, cyclopropyl, Bun, Bui, Bus, But/sup