19326-23-9

Upstream product

• 108-95-2 phenol 
• 22077-44-7 O,O-diphenyl phosphorochloridothioate 

Downstream Products

• 13561-75-6 Isocyanatothiophosphorsaeure-O,O-diphenylester 
• 90430-78-7 tetraphenyl imidothiodiphosphate 
• 13561-77-8 Oxalsaeure-N,N'-bis-(O,O-diphenyl-thiophosphono)-diamid 
• 945492-05-7 N-benzylidene-O,O-diphenylthiophosphoramide 
• 13557-08-9 N-Phenyl-N'--harnstoff 
• 13557-05-6 Thiophosphorsaeure-O,O-diphenylester-methoxycarbonylamid 
• 13604-54-1 N-Benzoyl-O,O-diphenyl-amidothiophosphorsaeure 
• 788758-10-1 amidothiophosphoric acid O-phenyl ester 
• 23575-34-0 -bis--phosphoran 
• 76711-24-5 C₉H₂₁Cl₂P 
• 90430-77-6 O,O',O'',O'''-tetraphenyl-μ-imido-dithiophosphate 
• 55339-56-5 C₃₀H₂₅NO₂P₂S 
• 31650-43-8 C₃₆H₃₀NO₂P₃S 
• 37390-51-5 N-(Fluorenyliden-⁽⁹⁾-methyl)-O,O-diphenyl-thiophosphorsaeureamid 

Relevant academic research and scientific papers

The synthesis and evalution of novel aryl-substituted dithioimidophosphonates as an extrantant for metals

A novel series of O,O′,O″,O?- tetraaryldithioimidophonates [(ArO)2PS]2NH 4 were synthesized by the reaction of O,O,-diaryl phosphorochlorothionates 2 and diarylphosphonothioic amide under a strong basic condition. The key intermediat

New mixed-donor unsymmetrical P-N-P ligands and their palladium(II) complexes

Unsymmetrical bidentate ligands R2P(E)-N(H)-P(E′)R′2 [R, R′ = Ph, OPh, iPr; E, E′ = O, S, Se] have been synthesised using the condensation reaction of an amino compound, R2P(E)NH2 [R = PhO, Ph; E = O, S, Se], with a phosphorus electrophile, R′2P(E′)C1 [R′ = iPr, Ph, OPh; E′ = O, S, Se]. Deprotonated ligands (with KOtBu) can be treated with Pd(OAc)2 to give [Ph2P(S)-N-P(O)(OPh)2]2Pd, [iPr2P(S)-N-P(O)(OPh)2]2Pd and [Ph2P(S)-N-P(S)(OPh)2]2Pd, which show either four-membered or six-membered chelate rings. The new compounds were studied spectroscopically (NMR, IR and Raman) and by X-ray crystallography.