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Ethyl phenyl phosphorodithiote, also known as EPN or O-ethyl O-phenyl S,S-dipropyl phosphorodithioate, is an organophosphorus compound primarily used as an insecticide and acaricide. It is a colorless to pale yellow liquid with a garlic-like odor and is highly toxic to both mammals and insects. EPN works by inhibiting the enzyme acetylcholinesterase, which disrupts the nervous system of the target pests, leading to paralysis and death. Due to its high toxicity and potential environmental risks, its use has been restricted or banned in many countries.

947-34-2

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947-34-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 947-34-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,4 and 7 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 947-34:
(5*9)+(4*4)+(3*7)+(2*3)+(1*4)=92
92 % 10 = 2
So 947-34-2 is a valid CAS Registry Number.

947-34-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name diethoxy-phenylsulfanyl-sulfanylidene-λ<sup>5</sup>-phosphane

1.2 Other means of identification

Product number -
Other names Ethyl phenyl phosphorodithiote

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:947-34-2 SDS

947-34-2Downstream Products

947-34-2Relevant academic research and scientific papers

Practical Reagents and Methods for Nucleophilic and Electrophilic Phosphorothiolations

Kovács, Szabolcs,Bayarmagnai, Bilguun,Aillerie, Alexandre,Goo?en, Lukas J.

supporting information, p. 1913 - 1918 (2018/03/30)

New late-stage phosphorothiolation methods are disclosed that allow the efficient transfer of SP(O)(OR)2 groups to diversely functionalized substrates using nucleophilic and electrophilic reagents. The nucleophilic reagent, tetramethylammonium O,O-dimethyl phosphorothioate, was synthesized in near-quantitative yield from Me3SiP(O)(OMe)2, elemental sulfur and Me4NF. Its umpolung with N-bromophthalimide provided the electrophilic reagent, O,O-dimethyl-S-(N-phthalimido)phosphorothioate. Complementary methods based on these reagents enable the phosphorothiolation of diversely functionalized alkyl halides, arenediazonium salts, arylboronic acids and electron-rich arenes in good yields under mild conditions. (Figure presented.).

Reactions of Aromatic Diazonium Salts with Esters of Acrylic and Methacrylic Acids in the Presence of O,O′-Diethyl Phosphodithioates

Grishchuk,Gorbovoi,Kudrik,Ganushchak,Kaspruk

, p. 362 - 364 (2007/10/03)

Alkyl 2-(diethoxythiophosphorylthio)-2-phenylpropionates were prepared by reaction of aromatic diazonium salts with esters of acrylic and methacrylic acids in the presence of potassium O,O′-diethyl dithiophosphate in a water-acetone (1 : 2) medium. The reaction is accompanied by formation of aryl O,O′-diethyl phosphodithioates. The diethoxythiophosphorylthioarylation of acrylates readily occurs in the absence of copper salts, thus providing an example of a noncatalytic reaction of diazonium salts with unsaturated compounds in the presence of foreign nucleophiles.

SYNTHESIS OF O,O-DIALKYL S-PHENYL PHOSPHOROTHIOLATES- AND DITHIOLATES

Yousif, N. M.,Gadalla, K. Z.,Yassin, S. M.

, p. 261 - 263 (2007/10/02)

Benzenesulfenyl chloride reacts with trialkylphosphite to give O,O-dialkyl S-phenyl phosphorothiolates 3 in high yield.Compounds 3 are thiated using 1,3-dithia 2,4-diphosphetane 2,4-disulfides 6 to produce O,O-dialkyl S-phenyl phosphorodithiolates 7 in ne

Method for preparation of phosphorus polysulfides

-

, (2008/06/13)

A process for the preparation of phosphorus polysulfides which comprises reacting a compound containing one or more --SH radicals with a sulfenamide characterized by the presence of a carbonyl group adjacent to the sulfenamide nitrogen wherein one or both of the SH compound and sulfenamide contains a phosphoryl moiety.

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