1449519-96-3

Basic information

• Product Name: diethyl (2-(1,3-dioxoisoindolin-2-yl)-2-((4-fluorobenzyl)oxy)propyl)phosphonate
• CAS NO: 1449519-96-3
• Molecular Weight: 449.416
• Mol File: 1449519-96-3.mol

Chemical Properties

• CAS DataBase Reference: diethyl (2-(1,3-dioxoisoindolin-2-yl)-2-((4-fluorobenzyl)oxy)propyl)phosphonate(CAS DataBase Reference)
• NIST Chemistry Reference: diethyl (2-(1,3-dioxoisoindolin-2-yl)-2-((4-fluorobenzyl)oxy)propyl)phosphonate(1449519-96-3)
• EPA Substance Registry System: diethyl (2-(1,3-dioxoisoindolin-2-yl)-2-((4-fluorobenzyl)oxy)propyl)phosphonate(1449519-96-3)

Safety Data

• Hazardous Substances Data: 1449519-96-3(Hazardous Substances Data)

Upstream product

• 85-44-9 phthalic anhydride 
• 4192-28-3 Phth-L-Ala-OH 
• 459-56-3 4-fluorobenzylic alcohol 
• 1449519-80-5 (S)-diethyl (1-diazo-2-(1,3-dioxoisoindolin-2-yl)propyl)phosphonate 
• 4306-25-6 (S)-2-phthalimidopropionyl chloride 
• 151397-24-9 (S)-diethyl(2-(1,3-dioxoisoindolin-2-yl)propanoyl)phosphonate 
• 1449519-79-2 (S)-diethyl(2-(1,3-dioxoisoindolin-2-yl)-1-(2-tosyl-hydrazono)propyl)phosphonate 

Relevant articles and documents

Combined C-H functionalization/O-H insertion reaction to form tertiary β-alkoxy substituted β-aminophosphonates catalyzed by [Cu(MeCN) 4]PF6

The copper-catalyzed C-H functionalization/O-H insertion reaction of α-diazophosphonates with alcohols has been developed with iodine as an additive. In order to understand this reaction, we present here a possible mechanism for the combined reaction. This process provides straightforward access to tertiary β-alkoxy substituted β-aminophosphonate derivatives with moderate to good yields. The Royal Society of Chemistry.