25626-89-5

Basic information

• Product Name: O,O-diethyl-N-ethyl-N-phenyl-phosphoramidate
• Synonyms: O,O-diethyl-N-ethyl-N-phenyl-phosphoramidate
• CAS NO: 25626-89-5
• Molecular Weight: 257.269
• Mol File: 25626-89-5.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: O,O-diethyl-N-ethyl-N-phenyl-phosphoramidate(CAS DataBase Reference)
• NIST Chemistry Reference: O,O-diethyl-N-ethyl-N-phenyl-phosphoramidate(25626-89-5)
• EPA Substance Registry System: O,O-diethyl-N-ethyl-N-phenyl-phosphoramidate(25626-89-5)

Safety Data

• Hazardous Substances Data: 25626-89-5(Hazardous Substances Data)

Upstream product

• 2397-47-9 triethyl N-phenylphosphorimidate 
• 75-03-6 ethyl iodide 
• 74-96-4 ethyl bromide 
• 1445-38-1 diethyl phenylphosphoramidate 
• 147672-01-3 C₁₂H₅⁽²⁾H₁₅NO₃P 
• 103-69-5 N-ethyl-N-phenylamine 
• 122-52-1 triethyl phosphite 
• 54635-88-0 phenyl-imidophosphoric acid tributyl ester 
• 102968-99-0 tris(isopropyloxy)phenyliminophosphane 
• 133827-73-3 trideuteromethyl phenylimidophosphate 
• 762-04-9 phosphonic acid diethyl ester 

Downstream Products

• 73755-65-4 (OC₂H₅)2P(O)N(C₂H₅)C₆H₅(BF₃) 

Relevant articles and documents

Electrochemical phosphorylation of arenols and anilines leading to organophosphates and phosphoramidates

A practical phosphorylation for generating organophosphates and phosphoramidatesviaelectrochemical dehydrogenative cross-coupling of P(O)H compounds with arenols and anilines is disclosed. This method involves using inorganic iodide salts as both redox catalysts and electrolytes in an undivided cell without the addition of oxidants or bases. A preliminary mechanistic study suggests that radicals are not involved in this process. This method is green and eco-friendly and has good functional group tolerance, high yields and broad substrate scope, with the potential for practical synthesis.

GC-MS STUDY OF THE IMIDE - AMIDE REARRANGEMENT

The imide - amide rearrangement of trialkyl arylimidophosphates by the action of catalytic amounts of boron trifluoride etherate proceeds at least partially by an intermolecular mechanism.Keywords: capillary gas-liquid chromatography/mass spectrometry, im

IMIDE-AMIDE REARRANGEMENT UNDER THE INFLUENCE OF BORON TRIFLUORIDE ETHERATE

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