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Diethyl S-(4-chlorophenylthio)methyl phosphorothionate, also known as Chlorpyrifos, is a widely used organophosphate insecticide. It is a colorless to pale yellow oily liquid with a chemical formula of C9H11Cl3NO3PS. Chlorpyrifos works by inhibiting the enzyme acetylcholinesterase in the nervous system of insects, leading to their paralysis and eventual death. It is effective against a broad spectrum of pests, including aphids, mites, and various types of beetles. However, due to its potential health risks and environmental concerns, its use has been restricted or banned in several countries.

3851-88-5

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3851-88-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3851-88-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,5 and 1 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3851-88:
(6*3)+(5*8)+(4*5)+(3*1)+(2*8)+(1*8)=105
105 % 10 = 5
So 3851-88-5 is a valid CAS Registry Number.

3851-88-5Downstream Products

3851-88-5Relevant academic research and scientific papers

Reaction of Phosphinyl and Phosphinothioyl Disulfides with Diazomethane

Miyamoto, Toru,Yamamoto, Izuru

, p. 2581 - 2586 (2007/10/02)

Four kinds of 4-substituted phenyl diethoxyphosphinyl disulfide (substituents: H, CH3, C2H5, Cl) and phenyl diethoxyphosphinothioyl disulfide reacted readily with diazomethane.The phosphinyl disulfides produced diethyl (4-substituted phenylthio)methyl phosphorothionate and the isomer, diethyl S-(4-substituted phenylthio)methyl phosphorothiolate, as the main products, whereas the phosphinothioyl disulfide produced only diethyl S-(phenylthio)methyl phosphorodithioate.The possible mechanism involved is as follows: the S-S bond in (EtO)2P(X)-S-S-C6H4R (X=O or S) is cleaved by nucleophilic attack of diazomethane at the sulfur atom bonded to the phenyl group to produce and (+)N2CH2-S-C6H4R; the latter reacts with the former with loss of nitrogen; therefore, when X is O, two compounds, (EtO)2P(S)-O-CH2-S-C6H4R and (EtO)2P(O)-S-CH2-S-C6H4R, are produced, when X is S, only (EtO)2P(S)-S-CH2-S-C6H4R is obtained.

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