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Dithiophosphoric acid O-methyl ester S-methylcarbamoylmethyl ester; compound with dimethyl-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

16284-76-7

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16284-76-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16284-76-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,2,8 and 4 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 16284-76:
(7*1)+(6*6)+(5*2)+(4*8)+(3*4)+(2*7)+(1*6)=117
117 % 10 = 7
So 16284-76-7 is a valid CAS Registry Number.

16284-76-7Downstream Products

16284-76-7Relevant academic research and scientific papers

Naeherungsverfahren zur Ermittlung von Teilgeschwindigkeitskonstanten eines komplexen, linear abhaengigen Reaktionsmodells

Fuellbier, Barbara,Haberland, Detlef

, p. 52 - 56 (2007/10/02)

A system of linear dependent competitive secondary reactions is regard to, for the kinetical investigation of the synthesis of dimethoate.An analytical solution of this simultane differential equation system is not possible.Various most integral methods of approximation for the solution of this problem are proposed and their usefulness are tested on the basis of experimental data.A complete solution of the differential equations, which is permitted to test the quality of the applied methods of approximations, are obtained by French-transformation.A good correspondence between experimental and calculated data is obtained by using a numerical procedure of Runge-Kutta.

Kinetic Investigations on the Aminolysis Reaction of the Dithiophosphoric Esters with Monomethylamine in Binary Methanol/Water - Mixtures

Fuellbier, B.,Klemmer, K.,Wettengel, A.,Haberland, D.

, p. 911 - 918 (2007/10/02)

The influence of the solvent polarity on the aminolysis reaction between O,O-dimethyl-S-(methoxycarbonylmethyl)-dithiophosphoricacidester (1) and monomethylamine, which is the main reaction of the "Dimethoate" synthesis, is investigated.The observed effects are compared with those of the alkylation of these esters by monomethylamine.Both reactions show a similar dependence on the solvent polarity.

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