55249-23-5

Basic information

• Product Name: Phosphinoselenoic chloride, diphenyl-
• CAS NO: 55249-23-5
• Molecular Formula: C12H10ClPSe
• Molecular Weight: 299.598
• Mol File: 55249-23-5.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Phosphinoselenoic chloride, diphenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Phosphinoselenoic chloride, diphenyl-(55249-23-5)
• EPA Substance Registry System: Phosphinoselenoic chloride, diphenyl-(55249-23-5)

Safety Data

• Hazardous Substances Data: 55249-23-5(Hazardous Substances Data)

Upstream product

• 1079-66-9 chloro-diphenylphosphine 

Downstream Products

• 486429-67-8 P,P-diphenylphosphinoselenothioic acid S₀[2-(trimethylsilyl)ethyl] ester 
• 97270-40-1 C₁₂H₁₁PSSe*C₄H₁₁N 
• 97270-41-2 C₁₂H₁₁PSSe*C₅H₁₁N 
• 97270-39-8 C₁₂H₁₁PSSe*C₆H₁₃N 
• 97270-42-3 C₁₂H₁₁PSSe*C₆H₇N 
• 38117-54-3 cyclopentadienyl iron(II) dicarbonyl dimer 
• 1059091-57-4 C₁₆H₁₉PSe₂ 
• 1059091-49-4 C₁₈H₁₅PSe₂ 
• 1059091-54-1 C₁₉H₁₇OPSe₂ 
• 1059091-55-2 C₂₁H₂₁PSe₂ 
• 1159596-29-8 Se-benzyl diphenyldiselenophosphinate 
• 1316847-31-0 N,N′-(ethane-1,2-diyl)bis(P,P-diphenylphosphinoselenoic amide) 
• 1316847-47-8 ethyl diphenylselenophosphinic glycylglycinate 
• 1316847-24-1 C₃₀H₂₉N₂O₃PSe 

Relevant articles and documents

New selenium-based iniferter agent for living free radical polymerization of styrene under UV irradiation

P,P-Diphenyl phosphinodiselenoic acid benzyl ester was synthesized and used as a mediator for the polymerization of styrene under UV-vis irradiation. Moderately controlled evidence was found: linear polymerization kinetics, linear evolution of molecular w

Synthesis of phosphinodiselenoic acid esters and their application as RAFT agents in styrene polymerization

Phosphinodiselenoic acid esters are synthesized from the reaction of chlorodiphenylphosphine and aryl- or alkyl-magnesium bromide in the presence of selenium powder. They are employed as RAFT agents in thermally initiated, styrene polymerization. The phos

Preparation and Some Reactions of Thioacyl Diphenylthiophosphinoyl and Thioacyl Diphenylphosphino Sulfides

The reaction of sodium or caesium dithiocarboxylates with diphenylthiophosphinic and diphenylselenophosphinic chlorides gives purple thioacyl diphenylthiophosphinoyl 5 and dark green thioacyl diphenylselenophosphinoyl sulfides 6, which are useful thioacylating reagents under mild reaction conditions.Thioacyl diphenylphosphino sulfides 22, which can be obtained by the similar method using diphenylphosphinous chlorides, react with methanol to yield the corresponding methyl dithiocarboxylates 15, while the reactions of 22 with N-chlorosuccinimide lead to hitherto unknown N-(thioacetylthio)succinimides 28.