13031-01-1

Upstream product

• 84531-30-6 4a,8a-bis(p-nitrophenylazo)decaline 

Downstream Products

• 7125-60-2 1(7)-bicyclo<5.3.0>decene 
• 110654-34-7 11-p-Tolyl-11-aza-tricyclo[5.3.1.0^1,7]undecan-2-one 
• 110654-35-8 11-(4-Bromo-phenyl)-11-aza-tricyclo[5.3.1.0^1,7]undecan-2-one 
• 104000-90-0 10-(2,4,6-Trimethyl-phenyl)-8-oxa-9-aza-tricyclo[5.3.3.0^1,7]tridec-9-en-2-one 
• 104000-91-1 10-(2,6-Dichloro-phenyl)-8-oxa-9-aza-tricyclo[5.3.3.0^1,7]tridec-9-en-2-one 
• 104000-89-7 10-Phenyl-8-oxa-9-aza-tricyclo[5.3.3.0^1,7]tridec-9-en-2-one 
• 110672-22-5 8,10-Diphenyl-8,9-diaza-tricyclo[5.3.3.0^1,7]tridec-9-en-2-one 
• 110672-27-0 11-Phenyl-11-aza-tricyclo[5.3.1.0^1,7]undecan-2-one 
• 110672-23-6 8-Phenyl-10-p-tolyl-8,9-diaza-tricyclo[5.3.3.0^1,7]tridec-9-en-2-one 
• 110672-25-8 10-(4-Chloro-phenyl)-8-phenyl-8,9-diaza-tricyclo[5.3.3.0^1,7]tridec-9-en-2-one 
• 275-51-4 azulene 
• 17647-77-7 4-methylazulene 
• 62547-99-3 Δ⁴⁽¹⁰⁾-octahydroazulene 

Relevant academic research and scientific papers

Study on the Transannular Lead Tetraacetate Oxidation of Some Medium-sized Ring Diketone Bis(arylhydrazones)

Oxidation of bis(arylhydrazones) 1a-d of 1,5-cyclooctanedione with lead tetraacetate mainly leads, via a transannular reaction, to the corresponding bicyclic bis(arylazo) compounds 3a-d, whereas bis(arylhydrazones) 2a-d of 3,8-cyclodecadiene-1,6-dione under the same conditions mainly give monocyclic bis(acetoxy)bis(arylazo) products 6a-d.The reaction of bis(arylazo) derivatives 3 with sulfuric acid is also examined.