80413-42-9

Basic information

• Product Name: Acetamide, 2-(diphenylphosphinyl)-N,N-diethyl-
• CAS NO: 80413-42-9
• Molecular Formula: C18H22NO2P
• Molecular Weight: 315.352
• Mol File: 80413-42-9.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: Acetamide, 2-(diphenylphosphinyl)-N,N-diethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Acetamide, 2-(diphenylphosphinyl)-N,N-diethyl-(80413-42-9)
• EPA Substance Registry System: Acetamide, 2-(diphenylphosphinyl)-N,N-diethyl-(80413-42-9)

Safety Data

• Hazardous Substances Data: 80413-42-9(Hazardous Substances Data)

Upstream product

• 719-80-2 Ethyl diphenylphosphinite 
• 2315-36-8 2-Chloro-N,N-diethylacetamide 
• 75-77-4 chloro-trimethyl-silane 
• 4559-70-0 Diphenylphosphine oxide 
• 1831-63-6 diphenylphosphorylacetic acid 
• 2283-11-6 hexaethylphosphoric triamide 
• 24630-80-6 diphenylphosphine oxide 
• 90-99-3 diphenylchloromethane 
• 2430-01-5 2-bromo-N,N-diethylacetamide 
• 20570-28-9 1-methoxy-1-methylethyl(diphenyl)phosphine oxide 

Downstream Products

• 1426585-16-1 2-[(diphenyl-N,N-diethylcarbamoylmethylphosphine oxide)methyl]pyridine 
• 1426585-11-6 2-[(diphenyl-N,N-diethylcarbamoylmethylphosphine oxide)methyl]pyridine N-oxide 
• 1426585-25-2 2,6-bis[(diphenyl-N,N-diethylcarbamoylmethylphosphine oxide)methyl]pyridine 
• 97775-18-3 TaF₅((C₆H₅)2POCH₂CON(C₂H₅)2) 

Relevant articles and documents

Carbamoylmethylphosphine oxide functionalised porous crosslinked polymers towards sequential separation of uranium (VI) and thorium (IV)

A new class of highly crosslinked porous polymeric materials with an ethylene glycol dimethacrylate (EGDMA) backbone appended with carbamoylmethylphosphineoxide (CMPO) ligands has been synthesized via precipitation polymerization. The polymers were charac

Reaction of (2-methoxyprop-2-yl)diphenylphosphine oxide with alkyl bromides

Treatment of (2-methoxyprop-2-yl)diphenylphosphine oxide with alkyl bromides affords alkyl(diphenyl)phosphine oxides in good yields.

ALKYLATION REACTIONS OF DIALKYL HYDROGEN PHOSPHITES AND DIARYLPHOSPHINE OXIDES UNDER PHASE-TRANSFER CONDITIONS

It was shown that phosphonates and tertiary phosphine oxides can be synthesized by the alkylation of acid phosphites and diarylphosphine oxides in a nonpolar solvent in presence of solid potassium hydroxide and potassium carbonate and also catalytic amounts of 18-crown ether (or in its absence). (Diarylphosphinyl)methyl ethers of mono- and oligo-etylene glycols were synthesized by the reactions of diaryl(chloromethyl)phosphine oxides with lithium glycolates