123560-30-5

Upstream product

• 1176903-74-4 2,4-diphenylcarbonohydrazide 
• 100-52-7 benzaldehyde 
• 100-63-0 phenylhydrazine 
• 52185-41-8 benzaldehyde α-chloroformylphenylhydrazone 
• 588-64-7 benzaldehyde phenylhydrazone 
• 591-50-4 iodobenzene 
• 52185-41-8 benzaldehyde 2-chloroformyl-2-phenylhydrazone 

Downstream Products

• 156216-46-5 tetrahydro-1-benzoyl-2,4,6-triphenyl-1,2,4,5-tetrazin-3(2H)-one 
• 1498310-20-5 1,5-diphenyl-3-(pyridin-2-yl)6-oxoverdazyl 
• 1498310-22-7 2,4-diphenyl-6-(pyridin-2-yl)-1,2,4,5-tetrazinan-3-one 
• 588-64-7 benzaldehyde phenylhydrazone 
• 19226-10-9 5-phenyl-3-phenyl-1,3,4-oxadiazol-2(3H)-one 
• 28740-63-8 5-methyl-3-phenyl-1,3,4-oxadiazol-2(3H)-one 
• 156216-45-4 tetrahydro-1-acetyl-2,4,6-triphenyl-1,2,4,5-tetrazin-3(2H)-one 

Relevant academic research and scientific papers

Profluorescent verdazyl radicals - synthesis and characterization

The synthesis and characterization of various 6-oxo-verdazyl radicals and their diamagnetic styryl radical trapping products are presented. It is shown that styryl radical trapping products derived from N-phenyl verdazyls show fluorescence whereas the N-m

N^N Pt(II) Bisacetylide Complexes with Oxoverdazyl Radical Ligands: Preparation, Photophysical Properties, and Magnetic Exchange Interaction between the Two Radical Ligands

To study the effect of a stable radical on the photophysical properties of a phosphorescent Pt(II) coordination framework and the intramolecular magnetic interaction between radical ligands in the N^N Pt(II) bisacetylide complexes, we prepared a series of

Kinetic investigation of thermal and photoinduced homolysis of alkylated verdazyls

The on-demand generation of stable organic radicals from the precursors can be considered as an essential challenge for the plethora of applications in various fields of science. In this contribution, we prepared a range of N-(methyl)benzyl derivatives of

New General Synthesis of Tetrahydro-1,2,4,5-tetrazin-3(2H)-one Derivatives and Stable 3,4-Dihydro-3-oxo-1,2,4,5-tetrazin-1(2H)-yl Radical Derivatives

Reactions of 2-chloroformylhydrazones of aromatic aldehydes or ketones 2 with various hydrazines were converted to monocarbonohydrazone derivatives 3 or 5 and/or tetrahydro-1,2,4,5-tetrazin-3(2H)-one derivatives 6,7.By oxidation with lead dioxide, compounds 6 were transformed into stable 3,4-dihydro-3-oxo-1,2,4,5-tetrazin-1(2H)-yl radical derivatives 8.

Verdazyls. Part 33. EPR and ENDOR Studies of 6-Oxo- and 6-Thioxoverdazyls. X-Ray Molecular Structure of 1,3,5-Triphenyl-6-oxoverdazyl and 3-tert-Butyl-1,5-diphenyl-6-thioxoverdazyl

A range of 6-oxoverdazyls 2b-h and 6-thioxoverdazyls 3a-c and 3e-h has been directly prepared by dehydrogenation of the corresponding 1,4,5,6-tetrahydro-1,2,4,5-tetrazin-3(2H)-ones 5b-h and thiones 7a-c and 7e-h with lead dioxide, potassium hexacyanoferra