96385-56-7

Usage

Chemical structure

The compound consists of a tetrazine ring and a combination of phenyl, methoxyphenyl, and nitrophenyl groups.

Tetrazine ring

The tetrazine ring is composed of four nitrogen atoms and one carbon atom, which gives the molecule unique properties and reactivity.

Aromatic characteristics

The presence of phenyl and nitrophenyl groups brings about aromatic characteristics.

Potential applications

The compound may have important applications due to its unique structure and properties.

Specific arrangement

The 1,2,5,6-tetrahydro-3-(4-methoxyphenyl)-1-(4-nitrophenyl)-5-phenylconfiguration implies a specific arrangement of these groups around the tetrazine core.

Stability

The arrangement of the groups around the tetrazine core can affect the molecule's stability.

Functions in chemical and biological processes

The specific arrangement of the groups may influence the molecule's potential functions in various chemical and biological processes.

4-Methoxyphenyl group

The presence of a 4-methoxyphenyl group in the compound may contribute to its unique properties and reactivity.

4-Nitrophenyl group

The 4-nitrophenyl group may also contribute to the compound's unique properties and reactivity.

Phenyl group

The phenyl group is a common structural element in many organic compounds and contributes to the aromatic characteristics of the molecule.

Upstream product

• 3637-11-4 1-hydroxy-2,2,6,6-tetramethyl-piperidin-4-one 
• 99910-02-8 C₂₁H₁₈N₅O₃ 
• 59-88-1 phenylhydrazine hydrochloride 
• 123-11-5 4-methoxy-benzaldehyde 
• 622-73-1 4-methoxybenzaldehydephenylhydrazone 
• 50-00-0 formaldehyd 
• 53451-82-4 3-(4-methoxyphenyl)-1-(4-nitrophenyl)-5-phenylformazan 

Downstream Products

• 3637-11-4 1-hydroxy-2,2,6,6-tetramethyl-piperidin-4-one 
• 99910-02-8 C₂₁H₁₈N₅O₃ 

Relevant academic research and scientific papers

Triarylverdazyl radicals as promising redox-active components of rechargeable organic batteries

A novel design of electroactive components of rechargeable organic batteries based on stable verdazyl radicals bearing various substituents is proposed. 3-Positioned aromatic substituents at the verdazyl moiety affect the reduction potentials and almost do not affect the oxidation potential, while 1-positioned aromatic substituents affect contrariwise the oxidation potential of this radical without any influence on the reduction potential. The acquired electrochemical data allowed us to reveal the structure—potential relationship for the cathodic and anodic processes, which provided the design of triarylverdazyl radicals possessing record-breaking parameters of the “electrochemical gap”.

DISSOCIATION ENERGY OF THE N-H BOND IN 2,6-DIARYL-4-PHENYL-1,2,3,4-TETRAHYDRO-SYM-TETRAZINES AND THE COMPARATIVE REACTIVITY OF SYM-TETRAZINYLS IN DEHYDROGENATION OF HYDRAZOBENZENE

The equilibrium constants in the reactions of 2,6-diaryl-4-phenyl-1,2,3,4-tetrahydro-sym-tetrazines with 2,2,6,6-tetramethyl-4-oxopiperidin-1-oxyl in heptane were determined by spectrophotometric and ESR methods.The dissociation energies of the N-H bond is the sym-tetrazines were determined.Results are given which indicate that the substituents in the phenyl ring at the C6 and N2 atoms have effects substantially different and opposite in sign on the thermochemical value of the dissociation energy of the N-H bond in sym-tetrazines.The sym-tetrazines with donatingsubstituents at the C6 atom and accepting substituents at the nitrogen atom are characterized by the largest dissociation energy for the N-H bond.The kinetics of the dehydrogenation of hydrazobenzene by sym-tetrazinyls in acetonitrile were investigated.It was found that there is an inverse relationship between the activation energies of the reaction and the dissociation energy of N-H bond in sym-tetrazines.The reaction mechanism is discused.