21538-58-9

Basic information

• Product Name: 7-bromo-1,3-diphenyl-1,4-dihydrobenzo[e][1,2,4]triazin-4-yl
• Synonyms: 7-bromo-1,3-diphenyl-1,4-dihydrobenzo[e][1,2,4]triazin-4-yl
• CAS NO: 21538-58-9
• Molecular Weight: 365.252
• Mol File: 21538-58-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 7-bromo-1,3-diphenyl-1,4-dihydrobenzo[e][1,2,4]triazin-4-yl(CAS DataBase Reference)
• NIST Chemistry Reference: 7-bromo-1,3-diphenyl-1,4-dihydrobenzo[e][1,2,4]triazin-4-yl(21538-58-9)
• EPA Substance Registry System: 7-bromo-1,3-diphenyl-1,4-dihydrobenzo[e][1,2,4]triazin-4-yl(21538-58-9)

Safety Data

• Hazardous Substances Data: 21538-58-9(Hazardous Substances Data)

Upstream product

• 21538-56-7 N-(4-bromophenyl)-N'-phenylbenzenecarbohydrazonamide 
• 14987-96-3 N-(4-bromophenyl)triphenyliminophosphorane 
• 952-53-4 1,3-diphenyl-2,3-diazaprop-2-en-1-one 

Downstream Products

• 1103917-89-0 6-bromo-1,2-diphenyl-1H-benzo[d]imidazole 

Relevant articles and documents

Preparation of Blatter Radicals via Aza-Wittig Chemistry: The Reaction of N-Aryliminophosphoranes with 1-(Het)aroyl-2-aryldiazenes

Reacting N-aryliminophosphoranes with 1-(het)aroyl-2-aryldiazenes in preheated diphenyl ether at ca. 150-250 °C for 5-25 min affords in most cases the 1,3-diaryl-1,4-dihydrobenzo[e][1,2,4]triazin-4-yls (aka Blatter radicals) in moderate to good yields. Al

Catalytic oxidation of N -phenylamidrazones to 1,3-Diphenyl-1,4-dihydro-1, 2,4-benzotriazin-4-yls: An improved synthesis of blatters radical

Blatters radical, 1,3-diphenyl-1,4-dihydro-1,2,4-benzotriazin-4-yl (1a, R =H), and several of its C-7 substituted analogues (R =CF3, Cl, Br, I, Me, OMe) were prepared in good-to-excellent yields through catalytic oxidation of the corresponding