63044-78-0

Basic information

• Product Name: N-benzyloxycarbonyl-9,10-dihydro-9,10-dimethyl-9,10-epoxyiminoanthracene
• Synonyms: N-benzyloxycarbonyl-9,10-dihydro-9,10-dimethyl-9,10-epoxyiminoanthracene
• CAS NO: 63044-78-0
• Molecular Weight: 371.436
• Mol File: 63044-78-0.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: N-benzyloxycarbonyl-9,10-dihydro-9,10-dimethyl-9,10-epoxyiminoanthracene(CAS DataBase Reference)
• NIST Chemistry Reference: N-benzyloxycarbonyl-9,10-dihydro-9,10-dimethyl-9,10-epoxyiminoanthracene(63044-78-0)
• EPA Substance Registry System: N-benzyloxycarbonyl-9,10-dihydro-9,10-dimethyl-9,10-epoxyiminoanthracene(63044-78-0)

Safety Data

• Hazardous Substances Data: 63044-78-0(Hazardous Substances Data)

Upstream product

• 3426-71-9 Benzyl N-hydroxycarbamate 
• 22566-43-4 9.10-dimethyl-9.10-dihydroanthracene 
• 781-43-1 9,10-dimethylanthracene 

Downstream Products

• 99027-97-1 N-benzyloxycarbonylazepine 
• 62995-08-8 19-benzyloxycarbonyl-6,14-dihydro-6β,14β-epoxyiminothebaine 

Relevant articles and documents

Hetero Diels–Alder Reaction and Ene Reaction of Acylnitroso Species in situ Generated by Hypoiodite Catalysis

As a first non-metal-catalyzed oxidation for the in situ generation of acylnitroso species, we describe the hypoiodite catalysis using tetra-n-butylammonium iodide as precatalyst with tert-butyl hydroperoxide or hydrogen peroxide as a terminal oxidant. Th

Copper-catalyzed aerobic oxidation of N-substituted hydroxylamines: Efficient and practical access to nitroso compounds

A general and efficient aerobic oxidation of N-substituted hydroxylamines is described. The mild reaction conditions employed provide a catalytic and sustainable alternative to stoichiometric oxidation methods to gain access to a range of nitroso compound

Development of new transition metal catalysts for the oxidation of a hydroxamic acid with in situ Diels-Alder trapping of the acyl nitroso derivative

New transition metal catalysts have been prepared and applied for in situ formation of acyl nitroso dienophiles. The Royal Society of Chemistry.