67463-35-8

Basic information

• Product Name: endo-4-phenyl-4-aza-10-oxatricyclo<5.2.1.0>dec-8-ene-3,5-dione
• Synonyms: endo-4-phenyl-4-aza-10-oxatricyclo<5.2.1.0>dec-8-ene-3,5-dione
• CAS NO: 67463-35-8
• Molecular Weight: 241.246
• Mol File: 67463-35-8.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: endo-4-phenyl-4-aza-10-oxatricyclo<5.2.1.0>dec-8-ene-3,5-dione(CAS DataBase Reference)
• NIST Chemistry Reference: endo-4-phenyl-4-aza-10-oxatricyclo<5.2.1.0>dec-8-ene-3,5-dione(67463-35-8)
• EPA Substance Registry System: endo-4-phenyl-4-aza-10-oxatricyclo<5.2.1.0>dec-8-ene-3,5-dione(67463-35-8)

Safety Data

• Hazardous Substances Data: 67463-35-8(Hazardous Substances Data)

Upstream product

• 6766-44-5 7-oxabicyclo<2.2.1>heptene-exo-2,3-dicarboxylic anhydride 
• 62-53-3 aniline 
• 110-00-9 furan 
• 941-69-5 N-phenyl-maleimide 

Downstream Products

• 110-00-9 furan 
• 941-69-5 N-phenyl-maleimide 

Relevant articles and documents

High Pressure, Temperature, and Solvent Effects on the Rate of the Diels-Alder Reaction of Furan with N-Phenylmaleimide

The effects of temperature, solvent nature, and high pressure on the rate of the Diels-Alder reaction of furan with N-phenylmaleimide were studied. A weak acceleration of the title reaction in proton-donor media was observed in comparison to other cycloaddition and ene reactions. The volumes of activation and reaction coincided within the experimental error, in keeping with the presumed cyclic transition state.

Expeditious 'on-water' cycloaddition between N-substituted maleimides and furans

Cycloaddition reactions between N-alkyl and N-aryl-substituted maleimides and furan derivatives have been carried out using the 'on-water' methodology. Transformations are faster and products can easily be isolated by simple workup protocols, often in qua

Photochemistry. IX. Formation of cyclopropenyl ketones and furans from pyridazine N oxides by irradiation

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