117881-35-3Relevant articles and documents
Kinetic study of hydrolytic decomposition of organophosphates and thiophosphate by N-hydroxyamides in cationic micellar media
Ghosh, Kallol K.,Sinha, Daliya,Satnami, Manmohan L.,Shrivastava,Dubey,Mundhara
, p. 726 - 730 (2007/10/03)
The nucleophilic hydrolyiic reactions p-nitrophenyl diphenyl phosphate (PNPDPP), p-nitrophenyl diethyl phosphate (Paraoxon) and p-nitrophenyl diethyl phosphorothioate (Parathion) with N-hydroxyamides have been investigated at 27 °C. With cationic micelles, rate enhancement has been observed on the nucleophilic attack at P center. All the rate surfactant profiles show typical micelle assisted bimolecular reactions. The interfacial ion exchange, control of the interfacial nucleophilc concentration and the reactivity at the micellar interface has been explained.
Thiolphosphoric acid-S-4-nitro-2-trichloromethylphenyl esters as fungicides
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, (2008/06/13)
New thiolphosphoric acid-S-4-nitro-2-trichloromethylphenyl esters of the formula STR1 where X denotes oxygen or sulfur, and R1 and R2 are identical or different and each denotes a substituted or unsubstituted aliphatic radical of 1 to 18 carbon atoms or a substituted or unsubstituted alicyclic radical of 5 to 18 carbon atoms, processes for their manufacture, fungicides containing these compounds as active ingredients, their manufacture, and processes for combating fungi with these novel compounds.