5055-11-8

Usage

Uses

Used in Organic Synthesis:
(2-chloroethyl)(diphenyl)phosphane is utilized as a reactant or reagent in organic synthesis, where its unique structure and reactivity contribute to the preparation of a diverse array of organic compounds and materials.
Used in Pharmaceutical Development:
In the pharmaceutical industry, (2-chloroethyl)(diphenyl)phosphane serves as a valuable component in the development of new drugs. Its ability to engage in various chemical reactions allows for the creation of innovative pharmaceutical compounds with potential therapeutic applications.
Used in Agrochemical Production:
Similarly, in agrochemicals, (2-chloroethyl)(diphenyl)phosphane is employed as a key intermediate in the synthesis of various agrochemical products. Its versatility in chemical reactions facilitates the production of effective compounds for agricultural applications.
Used in Specialty Chemicals:
(2-chloroethyl)(diphenyl)phosphane also finds application in the realm of specialty chemicals, where its unique properties are harnessed to create customized chemical products for specific industrial needs.

Upstream product

• 107-06-2 1,2-dichloro-ethane 
• 65567-06-8 lithium diphenylphosphide 
• 15475-27-1 potassium diphenylphosphine 
• 1079-66-9 chloro-diphenylphosphine 

Downstream Products

• 138710-61-9 (2-Diphenylphosphanyl-ethyl)-trimethyl-phosphonium; chloride 
• 23582-04-9 tetraphos 
• 603950-57-8 5-tert-butyl-4'-(2-diphenylphosphanylethylsulfanyl)-4-hydroxybiphenyl-3-carbaldehyde 
• 798548-39-7 [2-(4-bromo-phenylsulfanyl)-ethyl]-diphenyl-phosphane 
• 864228-26-2 (2-(2,4-dimethylphenylthio)ethyl)diphenylphosphine 
• 864228-25-1 diphenyl(2-((2,3,5,6-tetrafluorophenyl)thio)ethyl)phosphane 
• 919992-20-4 1-bromo-4-[2-(diphenylphophinothioyl)ethylsulfanyl]benzene 
• 919992-21-5 4-[2-(diphenylphophinothioyl)ethylsulfanyl]benzaldehyde 
• 104730-82-7 Mn(CO)3((C₆H₅)2PCH₂P(C₆H₅)2)((C₆H₅)2PCH₂CH₂Cl)⁽¹⁺⁾*ClO₄^(1-)=[Mn(CO)3((C₆H₅)2PCH₂P(C₆H₅)2)((C₆H₅)2PCH₂CH₂Cl)]ClO₄ 
• 79375-49-8 bromo(tetracarbonyl)[(2-chloroethyl)diphenylphosphan]rhenium 
• 1060676-12-1 4-(2-diphenylphosphanylethylthio)benzoic acid 
• 919992-40-8 (2-(mesitylthio)ethyl)diphenylphosphine 
• 227174-97-2 diphenyl(2-((4-fluorophenyl)thio)ethyl)phosphane 

Relevant academic research and scientific papers

Self-Assembly and Aggregation-Induced Emission in Aqueous Media of Responsive Luminescent Copper(I) Coordination Polymer Nanoparticles

Luminescent copper(I)-based compounds have recently attracted much attention since they can reach very high emission quantum yields. Interestingly, Cu(I) clusters can also be emissive, and the extension from small molecules to larger architecture could re

Reversible carbon monoxide binding at copper(I) P-S-X (X = N, O) coordination polymers

Reaction of Ph2PCH2CH2S(2-C 6H4NH2) (1) or Ph2PCH 2CH2S(2-C6H4OMe) (2) with CuCl and AgSbF6 in the presence of THF affords

Phosphino-indenyl complexes of nickel(II)

The BH3-protected phosphinoindenyl ligand indenyl(CH 2)2PPh2·BH3 was used in the preparation of (η5/3:η0-indenyl(CH 2)2PPh2·BH3)Ni(PPh 3)Cl, which has been characterized by NMR spectroscopy and X-ray diffraction studies. On the other hand, all attempts at preparing the closely related complex (η5/3:η1indenyl(CH 2)2PPh2)NiCl, in which the tethered phosphine moiety is coordinated to the Ni centre, were unsuccessful. One of these unsuccessful attempts yielded instead the novel indenyl-PCP pincer complex {KP,KC,KP-1,3-(CH2CH 2PPh2)2-2-indenyl}NiCl, which has been characterized by X-ray diffraction studies.

Synthesis of a new family of water-soluble tertiary phosphine ligands and of their rhodium(I) complexes; olefin hydrogenation in aqueous and biphasic media

The series of phosphonium phosphines (Ph2P(CH2)nPMe3>X (n = 2, 3, 6, 10; N = NO3-, Cl-, PF6-), henceforth II-, III-, VI- and X-phosphos respectively, have been prepared and characterized.The ligands react with 2 (NBD = norbornadiene) to form the complexes X, one of which, PF6, has been characterized crystallographically.The 1:1 complexes X react with a second equivalent of ligand to form the complexes X, which form very active olefin hydrogenation catalysts in aqueous and aqueous-organic biphasic systems.The effect of chain length on activity is very significant, the complex of VI-phosphos forming the most active catalyst.