73514-80-4

Upstream product

• 256-96-2 dibenzoazepine 
• 41216-97-1 (5H-dibenzo[b,f]azepin-5-yl)(phenyl)methanone 

Downstream Products

• 1019856-40-6 [3-(8-benzyl-8H-1-thia-8-aza-dibenzo[e,h]azulen-2-ylmethoxy)-propyl]dimethyl-amine 
• 1019856-27-9 [2-(8-benzoyl-8H-1-thia-8-aza-dibenzo[e,h]azulen-2-ylmethoxy)-ethyl]dimethylamine 
• 1019856-26-8 [3-(8-benzoyl-8H-1-thia-8-aza-dibenzo[e,h]azulen-2-ylmethoxy)-propyl]dimethylamine 
• 959056-07-6 5-benzoyl-5,11-dihydro-10H-dibenzo[b,f]azepin-10-one 
• 1326707-16-7 5-benzoyl-11-chloro-5H-dibenzo[b,f]azepine-10-carbaldehyde 
• 1019856-41-7 [2-(8-benzyl-8H-1-thia-8-aza-dibenzo[e,h]azulen-2-ylmethoxy)-ethyl]dimethylamine 
• 1019856-61-1 (8-benzoyl-8H-1-thia-8-aza-dibenzo[e,h]azulen-2-yl)methanol 
• 1019856-55-3 (8-benzyl-8H-1-thia-8-aza-dibenzo[e,h]azulen-2-yl)methanol 
• 1019856-89-3 ethyl 8-benzoyl-8H-1-thia-8-aza-dibenzo[e,h]azulene-2-carboxylate 
• 95037-76-6 5H-N-benzoyl-10,11-dihydro-trans-10,11-dihydroxydibenzazepine 

Relevant academic research and scientific papers

Synthesis and anti-inflammatory activity of 8H-1-thia-8-aza-dibenzo[e,h] azulenes

Figure represented. Synthesis of a novel class of fused heterotetracyclic compounds, 8H-1-thia-8-aza-dibenzo[e,h]azulenes (VII), is described. Starting N-benzoyl-protected 5H-dibenzo[b,f]azepine (XI, PG = Bz) was oxidized to 5-benzoyl-10,11-epoxy-10,11-di