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Phenyl diethoxyphosphinyl disulfide, also known as O,O-diethyl phenylphosphonodithioate, is an organophosphorus compound with the chemical formula C10H15OPS2. It is a colorless to pale yellow liquid with a pungent odor and is soluble in most organic solvents. phenyl diethoxyphosphinyl disulfide is primarily used as an intermediate in the synthesis of various pesticides, particularly organophosphorus insecticides, and as a reagent in the preparation of other organophosphorus compounds. Due to its potential toxicity and environmental impact, it is essential to handle phenyl diethoxyphosphinyl disulfide with caution and adhere to proper safety measures during its production, storage, and use.

7439-48-7

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7439-48-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7439-48-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,3 and 9 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7439-48:
(6*7)+(5*4)+(4*3)+(3*9)+(2*4)+(1*8)=117
117 % 10 = 7
So 7439-48-7 is a valid CAS Registry Number.

7439-48-7Relevant 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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