49838-39-3

Upstream product

• 38899-21-7 2,3,5,6-tetramethylnitrosobenzene 
• 981-18-0 triphenyl(phenylazo)methane 
• 77569-61-0 C₂₄H₂₀B^(1-)*C₁₇H₁₉N₂O₂S⁽¹⁺⁾ 
• 77569-58-5 C₂₄H₂₀B^(1-)*C₁₂H₁₆N₃O₃⁽¹⁺⁾ 
• 77569-55-2 C₂₄H₂₀B^(1-)*C₁₂H₁₈N₃O₂S⁽¹⁺⁾ 
• 77569-53-0 C₂₄H₂₀B^(1-)*C₁₅H₁₆N₃⁽¹⁺⁾ 
• 77569-57-4 C₂₄H₂₀B^(1-)*C₁₀H₁₂N₃O⁽¹⁺⁾ 
• 77593-13-6 C₂₄H₂₀B^(1-)*C₁₀H₁₃ClN₃⁽¹⁺⁾ 
• 77569-60-9 C₂₄H₂₀B^(1-)*C₁₁H₁₄N₃⁽¹⁺⁾ 
• 77569-56-3 C₂₄H₂₀B^(1-)*C₁₁H₁₆N₃⁽¹⁺⁾ 
• 77569-52-9 4-N,N-Diethylaminobenzendiazoniumtetraphenylborat 
• 3855-89-8 4-methoxybenzenediazonium tetraphenylborate 
• 3855-90-1 4-methylbenzenediazonium tetraphenylborate 
• 77569-59-6 2,5-Diethoxy-4-(N-morpholino)benzendiazonium-tetraphenylborat 

Relevant academic research and scientific papers

On the Formation of Radicals during the Photolysis of 4-N,N-Dialkylaminobenzene Diazonium Tetraphenylborates

The photolysis of 4-N,N-dialkylaminobenzene diazonium tetraphenylborates 1-11 in dichloromethane proceeds by an electron transfer between ion pairs forming radicals as primary products.Using e.s.r. spin trapping technique arenediazo, phenyl, 4-N,N-dialkylamino phenyl and substituted cyclohexadienyl radicals could be detected.