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"O,O-dimethyl O-(2,4-dinitrophenyl) phosphorothioate" is a chemical compound with the molecular formula C8H8NO6PS. It is an organophosphorus compound, specifically a phosphorothioate, and is known for its use as an insecticide. O,O-dimethyl O-(2,4-dinitrophenyl) phosphorothioate is characterized by its two methyl groups attached to the phosphorus atom and a 2,4-dinitrophenyl group attached to the sulfur atom. It was widely used in agriculture for controlling pests but has been phased out in many countries due to its high toxicity and potential environmental and health risks. The compound's chemical structure and properties make it a potent acetylcholinesterase inhibitor, which disrupts the nervous system of insects, leading to their death. However, its persistence in the environment and potential for bioaccumulation have led to concerns about its long-term effects on ecosystems and human health.

4901-40-0

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4901-40-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4901-40-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,0 and 1 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4901-40:
(6*4)+(5*9)+(4*0)+(3*1)+(2*4)+(1*0)=80
80 % 10 = 0
So 4901-40-0 is a valid CAS Registry Number.

4901-40-0Relevant academic research and scientific papers

Experimental and computational determination of Bronsted coefficients for equilibrium transfer of the O,O-dimethyl phosphorothioyl group between oxyanion nucleophiles

Edwards, David R.,Maxwell, Christopher I.,Harkness, Robert W.,Neverov, Alexei A.,Mosey, Nicholas J.,Stan Brown

supporting information; experimental part, p. 258 - 266 (2012/06/30)

An experimental determination of the βEq value for equilibrium transfer of the O,O-dimethyl phosphorothioyl group between oxyanion nucleophiles in water and methanol at 25 °C is presented. The respective βEq values in the two solvents are experimentally the same at -1.45 ± 0.08 and -1.39 ± 0.12. Based on the observation that the Bronsted correlation for the nucleophilic reaction of phenoxides in water with substrate 1d (dimethyl 4-nitrophenyl phosphorothioate, pKa HOAr of 7.14) is linear over the entire range of phenoxides employed (5.53 ≤ pKaNu ≤12.38), the reaction for phenoxide nucleophiles displacing phenoxide leaving groups is probably concerted. The obtained data allow one to calculate, for a symmetrical transition state involving 2,4,5-trichlorophenoxide as a nucleophile and leaving group, an approximately 60% P-OAr cleavage and about 40% P-Nuc bond formation. A computational method is presented for the rapid prediction of the βEq values for such processes in water and methanol, and the results are compared with known values from the literature. Copyright

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