1583285-58-8

Basic information

• Product Name: (Z)-4-(3-(diethoxyphosphoryl)-2-(1,3-dioxoisoindolin-2-yl)prop-1-en-1-yl)phenyl acetate
• CAS NO: 1583285-58-8
• Molecular Weight: 457.42
• Mol File: 1583285-58-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (Z)-4-(3-(diethoxyphosphoryl)-2-(1,3-dioxoisoindolin-2-yl)prop-1-en-1-yl)phenyl acetate(CAS DataBase Reference)
• NIST Chemistry Reference: (Z)-4-(3-(diethoxyphosphoryl)-2-(1,3-dioxoisoindolin-2-yl)prop-1-en-1-yl)phenyl acetate(1583285-58-8)
• EPA Substance Registry System: (Z)-4-(3-(diethoxyphosphoryl)-2-(1,3-dioxoisoindolin-2-yl)prop-1-en-1-yl)phenyl acetate(1583285-58-8)

Safety Data

• Hazardous Substances Data: 1583285-58-8(Hazardous Substances Data)

Upstream product

• 65594-96-9 O-Acetyl-N-phthaloyltyrosin 
• 6636-22-2 O-acetyl-L-tyrosine 
• 1583285-46-4 (S)-4-(3-diazo-3-(diethoxyphosphoryl)-2-(1,3-dioxoisoindolin-2-yl)propyl)phenyl acetate 
• 85-44-9 phthalic anhydride 

Relevant articles and documents

Unexpected stereoselective synthesis of (Z)-β-alkenyl substituted β-amino phosphonates through β,γ-dihydrogen shift reaction catalyzed by a copper(I) complex and iodine [Cu(MeCN)4]PF 6/I2

A series of dialkyl a-diazophosphonates has been prepared from natural amino acids. The diazo decomposition of these diazophosphonate compounds with tetrakis(acetonitrile)copper(I) hexafluorophosphate/iodine, [Cu(MeCN) 4]PF6/I2, as catalyst has been investigated. It was found that the diazo decomposition of dialkyl a-diazophosphonates gave a mixture of β,γ-dihydrogen shift and 1,2-hydride migration products and afforded β-alk- enyl-substituted β-amino phosphonates with the Z configuration. The mechanism of this novel diazo decomposition process was discussed.