101315-43-9

Basic information

• Product Name: (4-Methoxyphenyl)phenylessigsaeure-<1-(4-methoxyphenyl)-2-(nonafluorbutylsulfonyloxy)-2-phenylvinylester>
• CAS NO: 101315-43-9
• Molecular Weight: 748.62
• Mol File: 101315-43-9.mol

Chemical Properties

• CAS DataBase Reference: (4-Methoxyphenyl)phenylessigsaeure-<1-(4-methoxyphenyl)-2-(nonafluorbutylsulfonyloxy)-2-phenylvinylester>(CAS DataBase Reference)
• NIST Chemistry Reference: (4-Methoxyphenyl)phenylessigsaeure-<1-(4-methoxyphenyl)-2-(nonafluorbutylsulfonyloxy)-2-phenylvinylester>(101315-43-9)
• EPA Substance Registry System: (4-Methoxyphenyl)phenylessigsaeure-<1-(4-methoxyphenyl)-2-(nonafluorbutylsulfonyloxy)-2-phenylvinylester>(101315-43-9)

Safety Data

• Hazardous Substances Data: 101315-43-9(Hazardous Substances Data)

Upstream product

• 36913-91-4 nonaflyl anhydride 
• 3580-75-4 2-diazo-1-[4-(methyloxy)phenyl]-2-phenylethanone 

Relevant articles and documents

Reaction of Azibenzils with Nonofluorobutanesulfonic Anhydride

Reaction of azibenzils 1a - e with nonafluorosulfonebutanesulfonic anhydride (Nf2O) yields mainly vinylene bis(nonofluorobutanesulfonates) E,Z-2a - e and benzils 3a - e.The presence of a non-nucleophilic amine prevents decomposition of the azibenzils by traces of acid in the anhydride.Compounds 2 stem from an initial O-sulfonylation of the azibenzils, whereas C-sulfonylation perhaps leads to the benzils.Diazodiphenylmethane is decomposed by Nf2O to give tetraphenylethylene, benzophenone, and benzophenone azine.