80717-25-5

Upstream product

• 13118-95-1 phenyl-(p-methoxyphenyl)phosphinic acid 
• 459-64-3 4-methoxybenzenediazonium tetrafluoroborate 
• 644-97-3 Dichlorophenylphosphine 

Downstream Products

• 80717-32-4 O-(phenyl-p-methoxyphenylphosphinyl)acetone oxime 
• 80717-26-6 O-(phenyl-p-methoxyphenylphosphinyl)hydroxylamine 
• 80717-29-9 N-acetyl-O-(phenyl-p-methoxyphenylphosphinyl)hydroxylamine 
• 100926-14-5 C₁₄H₁₆NO₅PS 
• 100926-18-9 C₁₄H₁₆NO₃P 
• 100926-12-3 N-hydroxylamine 

Relevant academic research and scientific papers

Alkylesters and N,N-Dimethylaminoethylesters of Unsymmetrical Phosphinic Acids

The phosphinic acid chlorides 6 and 9 react in good yields with N,N-dimethylaminoethanol to the corresponding esters 3 and 10.Reaction of the phenylphosphonous acid esters 1 and 2 with arylbromides, heteroarylbromides and carboxylic acid chlorides give es

N-hydroxylamines: Influence of Substituents on the Competitive Migration of Aryl and Phenyl Groups in the Lossen-like Rearrangement of their O-Methanesulphonyl Derivatives

The N-hydroxylamines ArPhP(O)NHOH (4) (Ar=p-XC6H4; X=MeO, Me, Cl, NO2) have been prepared from the corresponding phosphinic chlorides (3) using O-(trimethylsilyl)hydroxylamine and converted into the O-methanesulphonyl derivatives

O-(Diphenylphosphinyl)hydroxylamine: Preparation and Some Characteristic Chemical Reactions

Hydroxylamine reacts with diphenylphosphinic chloride (1) in benzene (or aqueous dioxan) to give O-(diphenylphosphinyl)hydroxylamine (3) and not the N-phosphinyl compound (2) as was previously thought.Di-p-tolyl-, bis-p-methoxyphenyl-, and phenyl-p-methox