6591-42-0

Usage

Uses

Used in Rubber Industry:
Phosphine sulfide, cyclohexyldiphenylis used as a vulcanization accelerator for enhancing the process of rubber production. Its role in this application is crucial for improving the strength and elasticity of rubber, making it suitable for various end-use applications.
Used in Plastics and Polymers Industry:
In the plastics and polymers industry, Phosphine sulfide, cyclohexyldiphenylserves as a stabilizer in PVC and polyolefin compounds. Its inclusion helps to prevent degradation and extend the lifespan of these materials, ensuring their durability and performance over time.
Used in Organic Synthesis:
Phosphine sulfide, cyclohexyldiphenylis utilized as an intermediate in the synthesis of a variety of organic compounds. Its unique chemical properties make it a valuable component in creating complex organic molecules for different applications.
Used in Organic Chemistry as a Chemical Reagent:
As a chemical reagent, Phosphine sulfide, cyclohexyldiphenylplays a significant role in organic chemistry. It aids in various chemical reactions and processes, contributing to the advancement of research and development in the field.

Upstream product

• 931-51-1 cyclohexylmagnesiumchloride 
• 1079-66-9 chloro-diphenylphosphine 
• 13639-74-2 methyldiphenylphosphine sulfide 
• 829-85-6 diphenylphosphane 
• 108-93-0 cyclohexanol 
• 108-85-0 1-bromocyclohexane 
• 6372-42-5 cyclohexyldiphenylphosphine 
• 66295-78-1 C₁₈H₁₉PS 
• 6591-07-7 diphenylphosphane sulfide 
• 110-83-8 cyclohexene 
• 131379-54-9 1H-imidazole-1-carbothioic acid O-cyclohexyl ester 

Relevant academic research and scientific papers

Intramolecular nucleophilic substitution of ω-haloalkylphosphine derivatives

ω-Haloalkylphosphine derivatives undergo the intramolecular nucleophilic substitution reaction upon treatment with a strong base, yielding either cycloalkylphosphine derivatives or heterocyclic phosphine derivatives. The selectivity of the cyclization of

Facile non-catalyzed synthesis of tertiary phosphine sulfides by regioselective addition of secondary phosphine sulfides to alkenes

An atom-economic green synthesis of tertiary phsophine sulfides has been developed based on catalyst- and solvent-free addition of secondary phosphine sulfides to diverse terminal and internal alkenes (hept-1-ene, cyclohexene, styrenes, allyl alcohol, vin

Radical phosphination of organic halides and alkyl imidazole-1- carbothioates

Taking advantage of a radical-based methodology, mild and chemoselective phosphination reactions of organic halide and alkyl imidazole-1-carbothioates have been developed. The mild reaction conditions allow labile functional groups to survive during the reaction. Copyright

Radical addition reactions of diphenylphosphine sulfide

Radical additions of diphenylphosphine sulfide [Ph2P(S)H] to various C=C bonds offers a general, mild and efficient approach to alkyl(diphenyl)phosphine sulfides. Georg Thieme Verlag Stuttgart.

Palladium-catalyzed synthesis of vinyl phosphines from ketones

The palladium-catalyzed conversion of vinyl triflates to vinyl phosphines is reported. This process allows for the synthesis of vinyl phosphines from ketones. Selective enolization of a variety of ketones followed by trapping of the enolate as the vinyl triflate is reported. The vinyl triflates are then converted to the corresponding vinyl phosphine through palladium catalysis. The resulting vinyl phosphines can then be reduced to give alkyl phosphines.

Conformational Preference of the Diphenylthiophosphinoyl Group in Cyclohexane and in the 1,3-Dithian-2-yl Ring

The conformational energy (A value) of the diphenylthiophosphinoyl group in cyclohexane was determined from the incorporation of 13C NMR data of mobile cis-4-(diphenylthiophosphinoyl)-1-phenylcyclohexane (4) and conformationally fixed cis- (5) and trans-4