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Trithiophosphorous acid triethyl ester, also known as triethyl phosphorothioate or O,O-diethyl phosphorodithioate, is an organophosphorus compound with the chemical formula C6H15O2PS2. It is a colorless to pale yellow liquid with a pungent odor, insoluble in water but soluble in organic solvents. Trithiophosphorous acid triethyl ester is primarily used as an agricultural pesticide, specifically as a systemic insecticide, acaricide, and nematicide. It works by inhibiting the activity of acetylcholinesterase, an enzyme essential for the proper functioning of the nervous system in insects. Due to its effectiveness and low mammalian toxicity, trithiophosphorous acid triethyl ester has been widely used in the control of various pests in crops. However, it is important to handle this chemical with care due to its potential environmental and health risks, and to follow proper safety guidelines during its application.

688-62-0

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688-62-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 688-62-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,8 and 8 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 688-62:
(5*6)+(4*8)+(3*8)+(2*6)+(1*2)=100
100 % 10 = 0
So 688-62-0 is a valid CAS Registry Number.
InChI:InChI=1/C6H15PS3/c1-4-8-7(9-5-2)10-6-3/h4-6H2,1-3H3

688-62-0Relevant academic research and scientific papers

Synthesis of mixed phosphorotrithioates from white phosphorus

Huangfu, Xinlei,Zhang, Yue,Chen, Peiyun,Lu, Guozhang,Cao, Yinwei,Tang, Guo,Zhao, Yufen

supporting information, p. 8353 - 8359 (2020/12/29)

The first general and high-yielding synthesis of mixed phosphorotrithioates (R1S)2P(O)SR2 involving white phosphorus, disulfides, and alkyl halides is presented, which provides the shortest and environmentally benign method to synthesize these compounds of practical importance. Only one method for the formation of (R1S)2P(O)SR2 from elemental phosphorus has been developed. Here, with the use of KOH as a base and DMSO-toluene as a solvent, various disulfides couple readily with white phosphorus to give O-potassium S,S-dialkylphosphorotrithioates (R1S)2P(S)OK in almost quantitative yields, which react with alkyl halides to form (R1S)2P(O)SR2 in high yields. The reaction is characterized by the complete conversion of white phosphorus. Moreover, this method can be easily adapted to large-scale preparation. Our mechanistic data suggest that the attack of RSK on S,S,S-trialkyl phosphorotrithioates and subsequent C-S bond cleavage, the Michaelis-Arbuzov-like dealkylation, are the key steps in the formation of (R1S)2P(S)OK.

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