68899-50-3

Upstream product

• 627-42-9 2-chloroethyl methyl ether 
• 65567-06-8 lithium diphenylphosphide 
• 829-85-6 diphenylphosphane 
• 15475-27-1 potassium diphenylphosphine 

Downstream Products

• 74339-28-9 (β-methoxyethyl)diphenylbenzylphosphonium iodide 
• 23054-06-0 (2-Methoxyethyl)-methyl-diphenyl-phosphoniumiodid 
• 111557-09-6 trans-dihydridotris((2-methoxyethyl)diphenylphosphine-P;P;O,P)ruthenium(II) 
• 127261-08-9 chloro(η4-1,5-cyclooctadiene){(2-methoxyethyl)diphenylphosphane}rhodium(I) 
• 123880-99-9 (η4-1,5-cyclooctadiene)-cis-bis{(2-methoxyethyl)diphenylphosphane}rhodium(I)-hexafluoroantimonate 
• 128389-43-5 trans-dichlorobis{(2-methoxyethyl)diphenylphosphane}palladium(II) 
• 128412-19-1 bis((μ-chloro)chloro{(2-methoxyethyl)diphenylphosphane}palladium(II)) 
• 118962-95-1 bis(methoxyethyldiphenylphosphan-O,P)-platinum⁽⁰⁾ 
• 144804-24-0 chloro-cis-bis{diphenyl(2-methoxyethyl)phosphine-P;P',O'}rhodium(I) 
• 116449-70-8 diiodobis(methoxyethyldiphenylphosphane)cobalt(II) 
• 202335-45-3 mer-trichloro-cis-bis[diphenyl(methoxyethyl)phosphine-P;P',O']iridium(III) 
• 206060-96-0 dichloro(η(6)-hexamethylbenzene)[(methoxyethyl)diphenylphosphine-P]ruthenium(II) 
• 215544-58-4 RhCl(CO)((C₆H₅)2P(CH₂)2OCH₃) 
• 115557-49-8 tetracarbonyl{(2-methoxyethyl)diphenylphosphine-O,P}tungsten 

Relevant academic research and scientific papers

Convenient methods for the synthesis of a library of hemilabile phosphines

A series of novel functionalized phosphines of hemilabile character, R 2P(CH2)nZ, have been prepared from diarylphosphines using several synthetic methodologies. The synthetic methods include the alkylation of lithium diar

BIPHASE REDUCTION OF HEPTANAL AND CYCLOHEXANONE BY SODIUM FORMATE CATALYZED BY ETHER-PHOSPHINE RUTHENIUM(II) COMPLEXES

RuCl22 has efficiently catalyzed the reduction of cyclohexanone and heptanal by sodium formate in chlorobenzene-water, using cetylpyridinium bromide as the phase transfer catalyst.In both cases, the reduction was first order both in t

Neuartige basische Liganden fuer die homogenkatalytische Methanolcarbonylierung. X. Synthese, Eigenschaften und Komplexchemie mehrzahniger Alkoxyethylphosphane und ihr Verhalten als Steuerliganden bei der Methanolhydrocarbonylierung

Bi-, tri-, and quadridentate alkoxyethylphosphanes of the type R1nP(CH2CH2OR2)3-n are obtained from the corresponding phosphides M3-nPR1n (M=Li, Na/K; R1=Ph, Cy (=cyclo-C6H11)) and 1,2-alkoxychloroethanes ClCH2CH2OR2