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O,O-diethyl phenylsulfonylamidophosphate, also known as O,O-diethyl phenylsulfonylphosphoramidate, is an organophosphorus compound with the chemical formula C10H15O4PS. It is a colorless liquid with a density of 1.26 g/cm3 and a boiling point of 120°C at 0.1 mmHg. o,o-diethyl phenylsulfonylamidophosphate is primarily used as an insecticide and acaricide, targeting pests such as aphids, mites, and whiteflies. It works by inhibiting the activity of acetylcholinesterase, an enzyme essential for the proper functioning of the nervous system in insects. As a result, it disrupts the nervous system, leading to paralysis and death of the target pests. Due to its effectiveness and low mammalian toxicity, o,o-diethyl phenylsulfonylamidophosphate is widely used in agriculture to protect crops from various pests.

1467-28-3

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1467-28-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1467-28-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,6 and 7 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1467-28:
(6*1)+(5*4)+(4*6)+(3*7)+(2*2)+(1*8)=83
83 % 10 = 3
So 1467-28-3 is a valid CAS Registry Number.

1467-28-3Relevant academic research and scientific papers

Organophosphorus ligands with XPNSO skeleton (X = O, S) and their Pd(II) complexes. Crystal and molecular structure of [{XP(OEt)2}(O 2SR)]NH (X = O, R = Me, Ph; X = S, R = C6H 4Cl-4) and Pd[{SP(OEt)2}(O2SC6H 4Cl-4)N]2

Oltean, Dorel,P?llnitz, Alpar,Silvestru, Anca

, p. 67 - 75 (2013/05/08)

Several organophosphorus acids of type [{XP(OEt)2}(O 2SR)]NH [X = O, R = Me (1), Ph (2), C6H4CH 3-4 (3); X = S, R = C6H4Cl-4 (4)] were obtained by a method based on the reaction between (EtO)2P(X)NHLi and the corresponding organosulfonyl chloride. They were subsequently deprotonated with KOBut. Salt metathesis reactions between PdCl2 and the corresponding potassium salts K[{XP(OEt)2}(O2SR)N] [X = O, R = Me (5), Ph (6), C6H4CH3-4 (7); X = S, R = C6H4Cl-4 (8)] in a 1:2 molar ratio resulted in palladium(II) complexes of type Pd[{XP(OEt)2}(O2SR)N] 2 [X = O, R = Me (9), Ph (10), C6H4CH 3-4 (11); X = S, R = C6H4Cl-4 (12)]. In a similar way was obtained the palladium(II) complex Pd[(SPPh2)(O 2SPh)N]2 (13), using the appropriate reagents. All compounds were characterized by multinuclear NMR (1H, 13C, 31P) and infrared spectroscopy. The potassium salts and the palladium complexes were investigated also by mass spectrometry. Single-crystal X-ray diffraction studies revealed a layered supramolecular assembly in case of acid 1, a monomeric structure for compound 4, while in case of compound 2 dimeric associations are formed in the solid state by NH?OP hydrogen bonding. A trans-S,N-coordination pattern of the organophosphorus ligand was found in the palladium complex 12. Moreover, short Cl?H contacts result in a polymeric [Pd[{SP(OEt)2}(O2SC6H 4Cl-4)N]2]n chain.

THE APPLICATION OF PHASE-TRANSFER CATALYZED VERSION OF ATHERTON-TODD REACTION TO SULFONAMIDES

Lukanov, L. K.,Venkov, A. P.,Mollov, N. M.

, p. 767 - 774 (2007/10/02)

A number of sulfonylphosphoramidates have been prepared by phase-transfer catalyzed version of Atherton-Todd reaction.

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