1101835-58-8

Basic information

• Product Name: C₃₀H₂₀N₂O₈
• Synonyms: C₃₀H₂₀N₂O₈
• CAS NO: 1101835-58-8
• Molecular Weight: 536.497
• Mol File: 1101835-58-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: C₃₀H₂₀N₂O₈(CAS DataBase Reference)
• NIST Chemistry Reference: C₃₀H₂₀N₂O₈(1101835-58-8)
• EPA Substance Registry System: C₃₀H₂₀N₂O₈(1101835-58-8)

Safety Data

• Hazardous Substances Data: 1101835-58-8(Hazardous Substances Data)

Upstream product

• 79-37-8 oxalyl dichloride 
• 1079437-89-0 6-phenylbenzo[d][1,3]dioxole-5-carbaldehyde oxime 

Downstream Products

• 224-11-3 trisphaeridine 
• 3319-15-1 rac-1-(4-methoxyphenyl)-ethanol 

Relevant articles and documents

Dioxime oxalates; new iminyl radical precursors for syntheses of N-heterocycles

Symmetrical and unsymmetrical dioxime oxalates were prepared by treatment of oximes with oxalyl chloride. UV photolysis of these precursors was found to be an atom-efficient way of generating iminyl radicals. The process was most efficient for dioxime oxalates having aryl substituents attached to their C{double bond, long}N bonds. The method was useful for EPR spectroscopic study of iminyl and iminoxyl radicals. Photolyses in toluene solution, of dioxime oxalates containing alkenyl acceptor groups, yielded unsaturated iminyl radicals that ring closed to afford 3,4-dihydro-2H-pyrroles in good yields. Dioxime oxalates with biphenyl substituents also released iminyl radicals that ring closed onto the aromatic acceptor groups and, in acetonitrile solution, this approach provided a useful and atom-efficient method of making substituted phenanthridines.