21776-15-8

Usage

Uses

Used in Organic Synthesis:
Ethenyl(diphenyl)phosphane sulfide is used as a reagent in organic synthesis, particularly for the preparation of organophosphorus compounds. Its unique properties make it a valuable component in the creation of various chemical products.
Used in Plastics Industry:
As a stabilizer for PVC, ethenyl(diphenyl)phosphane sulfide plays a crucial role in enhancing the durability and stability of plastic materials, thereby improving their performance and longevity.
Used in Flame Retardancy:
Ethenyl(diphenyl)phosphane sulfide is recognized for its potential use as a flame retardant. It is being researched for its possible applications in fire-resistant materials, which could contribute to increased safety in various industries.
Used in Pharmaceutical Research:
Due to its antibacterial and antitumor properties, ethenyl(diphenyl)phosphane sulfide is being studied for potential use in medicine. Its ability to combat infections and inhibit tumor growth makes it a promising candidate for further research and development in the medical field.
However, it is important to handle ethenyl(diphenyl)phosphane sulfide with caution, as it may be irritant to the skin, eyes, and respiratory system. Proper safety measures should be taken to minimize any potential risks associated with its use.

Upstream product

• 2155-96-6 Diphenylvinylphosphine 
• 1079-66-9 chloro-diphenylphosphine 
• 63000-06-6 divinyltellane 
• 6591-07-7 diphenylphosphane sulfide 
• 1357196-43-0 2-[2-(diphenylphosphorothioyl)ethyl]tellanylethyl(diphenyl)phosphine sulfide 

Downstream Products

• 20545-24-8 5-diphenylphosphinothioyl-3-phenyl-4,5-dihydro-isoxazole 
• 54772-63-3 [2-(Diphenyl-phosphinothioyl)-ethyl]-phenyl-phosphane 
• 131480-25-6 cis-6,6-dimethyl-2-diphenylthiophosphinylhexahydropyrrolo<1,2-b>isoxazole 
• 131480-26-7 cis-6,6-dimethyl-3-diphenylthiophosphinylhexahydropyrrolo<1,2-b>isoxazole 
• 119987-34-7 diphenyl(isopentyl)phosphine sulphide 
• 1237539-67-1 PtI₂SP(C₆H₅)2C₆H₅(CH₃)2AsC₆H₅ 
• 1237539-69-3 C₂₀H₂₁PS 
• 1237539-68-2 C₂₆H₂₆AsPS 
• 1237539-61-5 PdBr₂SP(C₆H₅)2C₆H₅(CH₃)2AsC₆H₅ 
• 607-01-2 ethyl-diphenyl-phosphane 
• 33355-58-7 <2-(phenylphosphino)ethyl>diphenylphosphine 
• 2096-78-8 vinyldiphenylphosphine oxide 
• 125155-35-3 trans-2,3-diphenyl-4-diphenylthiophosphinyltetrahydroisoxazole 
• 20545-27-1 cis-2,3-diphenyl-5-diphenylthiophosphinyltetrahydroisoxazole 

Relevant academic research and scientific papers

Mass spectrometry and quantum chemical studies of the reaction of divinyl telluride with secondary phosphine sulfides: Synthesis of adducts

Mass spectrometry and quantum chemical studies of the reaction of divinyl telluride with diphenylphosphine sulfide have been carried out. Reaction proceeds under radical initiation (AIBN, 63-68 C, 2.5 h, THF, reactants molar ratio = 1:1) to afford the ant

Reaction of divinyl telluride with secondary phosphine chalcogenides

Divinyl telluride reacted with 2 equiv of diphenylphosphine sulfide in the presence of AIBN as radical initiator (63-68°C) to give the corresponding anti-Markovnikov adduct in 68% yield with high regioselectivity. Treatment of the addition product with aqueous hydrogen peroxide at room temperature afforded 71% of vinyldiphenylphosphine oxide. Radical addition of diphenylphosphine selenide to divinyl telluride (AIBN, 63-68°C) led to the formation of 1,1,3,3-tetraphenyldiphosphoxane 1,3-diselenide in 82% yield. Pleiades Publishing, Ltd., 2011.

Highly atom-economic one-pot formation of three different C-P bonds: General synthesis of acyclic tertiary phosphine sulfides

The reaction of benzothiadiphosphole 1 with an equimolar mixture of R 1MgBr and R2MgBr gave intermediate A′, which, after only 4-5 min, was treated with an equimolar amount of R3MgBr, giving the asymmetric phosphine PR1R2R3 in 45% overall yield (75-80% yield when R1 = R2 and 85-90% yield when R1 = R2 = R3) and the byproduct 6 in 90% yield. The treatment of 6 with PCl3 quantitatively regenerates the starting reagent 1. Treatment of the phosphines with elemental sulfur gave the corresponding sulfides.