947-34-2

Basic information

• Product Name: Ethyl phenyl phosphorodithiote
• CAS NO: 947-34-2
• Molecular Weight: 262.334
• Mol File: 947-34-2.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Ethyl phenyl phosphorodithiote(CAS DataBase Reference)
• NIST Chemistry Reference: Ethyl phenyl phosphorodithiote(947-34-2)
• EPA Substance Registry System: Ethyl phenyl phosphorodithiote(947-34-2)

Safety Data

• Hazardous Substances Data: 947-34-2(Hazardous Substances Data)

Upstream product

• 369-57-3 benzenediazonium tetrafluoroborate 
• 3454-66-8 potassium O,O-diethyldithiophosphate 
• 140-88-5 ethyl acrylate 
• 97-63-2 methyl methacrylate 
• 141-32-2 acrylic acid n-butyl ester 
• 62-53-3 aniline 
• 1068-22-0 diethyl dithiophosphate ammonium salt 
• 931-59-9 benzenesulfenyl chloride 
• 1889-58-3 O,O-diethyl S-phenyl phosphorothioate 
• 14744-12-8 diphenyl ethylphosphonite 
• 298-06-6 O,O-Diethyl hydrogen phosphorodithioate 
• 3111-52-2 potassium thiophenolate 
• 2524-04-1 diethyl phosphorochloridothioate 
• 2901-90-8 bis(diethoxyphosphoryl)disulphide 

Relevant articles and documents

Synthesis and study of antimicrobial properties of 1-(O,O′-diethyldithiophosphato)-1-alkoxycarbonyl-2-phenylethanes

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

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.

Method for preparation of phosphorus polysulfides

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.