13715-63-4

Usage

Chemical structure

The compound consists of a triazolidine-3,5-dione ring and an anthracenyl group.

Triazolidine-3,5-dione ring

A five-membered heterocyclic ring containing three nitrogen atoms and two oxygen atoms.

Anthracenyl group

A polycyclic aromatic hydrocarbon.

Potential applications

The compound has potential applications in the field of organic synthesis and medicinal chemistry due to its unique structure and reactivity.

Development of new drugs

It may be used in the development of new drugs.

Building block

It may be used as a building block for the synthesis of more complex organic molecules.

Further investigation

The specific properties and potential uses of the compound would need to be further investigated through research and experimentation.

Upstream product

• 1705-82-4 10-diazo-10H-anthracen-9-one 
• 4233-33-4 4-Phenyl-1,2,4-triazolidine-3,5-dione 

Relevant academic research and scientific papers

Investigations on Diazo Compounds and Azides, LII: Stable Azomethine Imine Dipoles from Diazo Compounds and 3H-1,2,4-Triazole-3,5(4H)-diones

The aryl-substituted diazo compounds 1a-h react with the triazolediones 2a-c at 20 deg C in benzene with loss of nitrogen to the stable azomethine imine dipoles 4a-p.Their 1,3-dipolar character is revealed in the addition of methanol and ethanol (4d-f -> 5a-f) as well as in cycloaddition reactions with dimethyl acetylenedicarboxylate (4d,e -> 6a,b) and phenyl isocyanate (4d -> 7).Bisdipoles are obtained by two different ways: Either bisdiazo compounds are reacted with 4-phenyl-3H-1,2,4-triazole-3,5(4H)-dione (12a,b + 2 2a -> 13a,b) or the bistriazoledione 14 is transformed into the bisdipoles 15a-d with diazo compounds (1a,c,d, and i).Dipole moments, molecular weights, IR, UV, 1H NMR, and 13C NMR spectroscopic data are in agreement with the dipole structures.

OBER DIE REAKTIVITAET VON 4-PHENYL-1,2,4-TRIAZOLIN-3,5-DION MIT DIAZOVERBINDUNGEN

The aryl substituted diazo compounds 1a-e react with the triazolindione 2 under the evolution of nitrogen and the formation of the stable dipoles 4a-e.The dipoles resulting from the reaction of 1f-k with 2 cannot be isolated (4f-k) but trapped with ethanol (5f-k).Diazo compounds possessing a butadiene unit (7a-d and 10) prefer Diels-Alder-reaction with 2 and yield the polycycles 9a-d and 11.