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p-Chlorophenyl dimethyldithiophosphinate is a chemical compound with the molecular formula C8H9ClPS2. It is an organophosphorus compound, specifically a dithiophosphinate, which is characterized by the presence of two sulfur atoms bonded to a central phosphorus atom. p-chlorophenyl dimethyldithiophosphinate is known for its potential use as a pesticide or an intermediate in the synthesis of other agrochemicals. It features a chlorophenyl group, which is a phenyl ring with a chlorine atom attached, and two methyl groups bonded to the phosphorus. The compound's structure and properties make it a candidate for applications in the chemical industry, particularly in the development of compounds with biological activity. However, it is important to note that the use and handling of such chemicals require careful consideration due to their potential environmental and health impacts.

5745-35-7

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5745-35-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5745-35-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,4 and 5 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5745-35:
(6*5)+(5*7)+(4*4)+(3*5)+(2*3)+(1*5)=107
107 % 10 = 7
So 5745-35-7 is a valid CAS Registry Number.

5745-35-7Downstream Products

5745-35-7Relevant academic research and scientific papers

Rhodium-Catalyzed Synthesis of Dialkyl(Heteroaryl)Phosphine Sulfides by Phosphinylation of Heteroaryl Sulfides

Arisawa, Mieko,Tazawa, Takeru,Ichinose, Wataru,Kobayashi, Haruki,Yamaguchi, Masahiko

supporting information, p. 3488 - 3491 (2018/09/14)

Dialkyl(heteroaryl)phosphine sulfides were synthesized by the rhodium-catalyzed exchange reaction of heteroaryl aryl sulfides and tetraalkyldiphosphine disulfides. The reaction has a broad applicability, giving diverse dialkyl(heteroaryl)phosphine sulfides containing five- and six-membered heteroaryl groups. Various dialkyl(heteroaryl)phosphines were obtained by desulfurization. (Figure presented.).

Rhodium-catalyzed thiophosphinylation and phosphinylation reactions of disulfides and diselenides

Arisawa, Mieko,Ono, Tetsuya,Yamaguchi, Masahiko

, p. 5669 - 5671 (2007/10/03)

Alkyl and aryl dithiophosphinates were synthesized by the reaction of disulfides with biphosphine disulfides in the presence of RhH(PPh 3)4 and 1,2-diphenylphosphinoethane (dppe). The catalyst also promoted synthesis of thiophosphinates and selenothiophosphinates from disulfides and diselenides.

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