62956-32-5

Basic information

• Product Name: Phosphonic acid, [4-(acetylamino)phenyl]-, diethyl ester
• Synonyms: Diethyl-4-acetamidophenylphosphonat;diethyl 4-acetamidophenylphosphonate;diethyl (4-acetamidophenyl)phosphonate
• CAS NO: 62956-32-5
• Molecular Formula: C12H18NO4P
• Molecular Weight: 271.253
• Mol File: 62956-32-5.mol
• Article Data: 15

Chemical Properties

• CAS DataBase Reference: Phosphonic acid, [4-(acetylamino)phenyl]-, diethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Phosphonic acid, [4-(acetylamino)phenyl]-, diethyl ester(62956-32-5)
• EPA Substance Registry System: Phosphonic acid, [4-(acetylamino)phenyl]-, diethyl ester(62956-32-5)

Safety Data

• Hazardous Substances Data: 62956-32-5(Hazardous Substances Data)

Upstream product

• 539-03-7 N-(4-chlorophenyl)acetamide 
• 762-04-9 phosphonic acid diethyl ester 
• 556-08-1 p-(acetylamino)benzoic acid 
• 622-50-4 4-Acetamido-1-iodobenzene 
• 122-52-1 triethyl phosphite 
• 103-84-4 Acetanilid 
• 15898-43-8 sodium 4-acetamidobenzenesulfinate 
• 32578-30-6 m-4-acetamidophenyl trifluoromethanesulfonate 
• 20502-85-6 diethyl hydrogen phosphite 
• 103-88-8 4-bromoacetanilide 

Downstream Products

• 42822-57-1 diethyl (4-aminophenyl)phosphonate 
• 5337-17-7 4-aminophenylphosphonic acid 

Relevant articles and documents

Catalyst-free phosphorylation of aryl halides with trialkyl phosphites through electrochemical reduction

A catalyst-free electrochemical cross-coupling reaction of aryl halides with trialkyl phosphite has been developed. This reaction proceeds in an undivided cell with a low-cost Ni anode and a graphite cathode under mild and neutral conditions. A wide range of functional groups are well-tolerated and the phosphorylated product can be obtained on the gram scale, showing that this transformation has the potential to be a valuable method for the construction of aromatic carbon-phosphorus bonds.

Manganese-Catalyzed and Mediated Synthesis of Arylphosphinates and Related Compounds

The free-radical arylation of H-phosphinates and related compounds was examined. A practical catalytic process with the air as the oxidant could not be found. However, an inexpensive and robust methodology was developed, using catalytic Mn(II) as the radi

Palladium-catalyzed desulfitative cross-coupling reaction of sodium arylsulfinates with H-phosphonate diesters

A novel and convenient palladium-catalyzed cross-coupling reaction of H-phosphonate diesters with sodium arylsulfinates was developed via desulfitation in the presence of silver carbonate and tetra-butylammonium chloride. This method is highly efficient and provides a rapid access to a broad spectrum of arylphosphonate diesters in good to excellent yields.