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Thiophosphoric acid O,O,O-triisopropyl ester, also known as tri-isopropyl phosphorothioate, is an organophosphorus compound with the chemical formula C9H21O3PS. It is a colorless liquid with a pungent odor and is used as an insecticide and acaricide in agriculture. The compound is formed by the esterification of thiophosphoric acid with isopropanol, resulting in a molecule that contains three isopropyl groups attached to a central phosphorus atom bonded to a sulfur atom. Thiophosphoric acid O,O,O-triisopropyl ester is known for its effectiveness in controlling a wide range of pests, including insects and mites, due to its ability to inhibit acetylcholinesterase, an enzyme essential for the proper functioning of the nervous system in these organisms. However, it is also considered to be toxic to humans and animals, and its use is subject to strict regulations to minimize potential health and environmental risks.

2464-03-1

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2464-03-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2464-03-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,6 and 4 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2464-03:
(6*2)+(5*4)+(4*6)+(3*4)+(2*0)+(1*3)=71
71 % 10 = 1
So 2464-03-1 is a valid CAS Registry Number.

2464-03-1Relevant academic research and scientific papers

The Kinetics and Mechanism of the Reaction of Tricoordinate Phosphorus Compounds with Diaryl Trisulfides

Hall, C. Dennis,Tweedy, Bruce R.,Kayhanian, Robert,Lloyd, John R.

, p. 775 - 779 (2007/10/02)

Kinetic data and activation parameters are reported for the reaction of a series of tricoordinate phosphorus compounds, , with diaryl trisulfides.The second-order rate coefficients for series of arylphosphines, phosphinites and phosphonites, correlate with the Hammett ? constants of the aryl substituents with ρ values of -1.1, -1.1 and -1.1 respectively and these results are discussed in terms of a biphilic mechanism analogous to that proposed for the reaction of tricoordinate phosphorus with S8.

Reactions of Group V Metal Compounds with Sulfur Trioxide

Ando, Fumio,Koketsu, Jugo,Ishii, Yoshio

, p. 3495 - 3499 (2007/10/02)

Trialkylphosphines react with equimolar amounts of sulfuric trioxide to form the 1:1 adducts R3P(1+)-SO3(1-).Trialkylarsines and -stibines undergo sulfur trioxide insertion reaction across the metal-carbon bond to give the trisulfonates of the metal M(OSO2R)3 (M=As,Sb).The reactions of trialkyl phosphites, with sulfur trioxide yield trialkyl phosphonates, trialkyl thiophosates, dialkyl alkylphosphonates, dialkyl sulfates, and polymers which contain phosphorus atoms.The reactions of trialkoxyarsines and -stibines result in the insertion of sulfur trioxide across the metal-oxygen bond to form the alkoxymetal alkylsulfates (RO)3-nM(OSO3R)n (M=As,Sb; n=1,2,3) depending on the stoichiometric ratios of the reagents used.Pyrolysis of the metal sulfates gives dialkyl sulfates and undistillable residues containing the metals.

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