1588513-04-5

Basic information

• Product Name: C₃₀H₃₂N₇O₆⁽¹⁺⁾*BF₄^(1-)
• Synonyms: C₃₀H₃₂N₇O₆⁽¹⁺⁾*BF₄^(1-)
• CAS NO: 1588513-04-5
• Molecular Weight: 673.432
• Mol File: 1588513-04-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₃₀H₃₂N₇O₆⁽¹⁺⁾*BF₄^(1-)(CAS DataBase Reference)
• NIST Chemistry Reference: C₃₀H₃₂N₇O₆⁽¹⁺⁾*BF₄^(1-)(1588513-04-5)
• EPA Substance Registry System: C₃₀H₃₂N₇O₆⁽¹⁺⁾*BF₄^(1-)(1588513-04-5)

Safety Data

• Hazardous Substances Data: 1588513-04-5(Hazardous Substances Data)

Upstream product

• 1588512-38-2 C₁₈H₂₃N₄O₅⁽¹⁺⁾*BF₄^(1-) 
• 453-71-4 3-nitro-4-fluorobenzoic acid 
• 16250-37-6 N-allylformamide 
• 1410063-79-4 C₁₉H₂₄N₅O₃⁽¹⁺⁾*BF₄^(1-) 
• 555-16-8 4-nitrobenzaldehdye 

Downstream Products

• 1588513-34-1 methyl 3-allyl-2-[4-(nitrooxy)phenyl]-4-oxo-10-(tetrahydro-2-furanylmethyl)-2,3,4,10-tetrahydrobenzo[4,5]imidazo[1,2-a][1,3,5]triazin-7-ylcarboxylate 

Relevant articles and documents

Regioselective piperidine-catalyzed tandem imination-isocyanate annulation to fused tricyclic triazines

A novel tandem imination-isocyanate-mediated annulation was explored. Ionic liquid-immobilized 2-aminobenzimidazoles react sequentially with aldehydes and isocyanates to give highly functionalized benzimidazole-embedded triazines. The second-stage transformation revealed that the formation of triazinone functionality is entirely regioselective to allow rapid assembly of biologically interesting tricyclic skeletons. In conjunction with the application of microwave irradiation and IL support, this method provides an efficient route to access substituted benzoimidazotriazines.