33906-65-9

Upstream product

• 536-90-3 m-Anisidine 
• 120952-16-1 2-(2,4-dinitrophenoxy)-N-ethylpyridinium tetraphenylborate 
• 106-49-0 p-toluidine 
• 104-94-9 4-methoxy-aniline 
• 99-98-9 4-amino-N,N-dimethylaniline 
• 62-53-3 aniline 
• 108-44-1 1-amino-3-methylbenzene 
• 106-50-3 1,4-phenylenediamine 
• 14485-20-2 lithium tetraphenylborate 
• 63717-74-8 Li⁽¹⁺⁾*(C₆H₅)3BH^(1-)=Li((C₆H₅)3BH) 
• 587-85-9 diphenylmercury(II) 
• 960-71-4 triphenylborane 
• 591-51-5 phenyllithium 

Downstream Products

• 960-71-4 triphenylborane 
• 207462-63-3 (C₅H₅)Fe(C₅H₄)C(CH₃)C₁₀H₇⁽¹⁺⁾*B(C₆H₅)4^(1-) = [(C₅H₅)Fe(C₅H₄)C(CH₃)C₁₀H₇][B(C₆H₅)4] 
• 72317-01-2 WH(CNC(CH₃)3)2((C₆H₅)2PCH₂CH₂P(C₆H₅)2)2⁽¹⁺⁾*B(C₆H₅)4^(1-)=[WH(CNC(CH₃)3)2((C₆H₅)2PCH₂CH₂P(C₆H₅)2)2]B(C₆H₅)4 
• 72316-97-3 WH(CNCH₃)2((C₆H₅)2PCH₂CH₂P(C₆H₅)2)2⁽¹⁺⁾*B(C₆H₅)4^(1-)=[WH(CNCH₃)2((C₆H₅)2PCH₂CH₂P(C₆H₅)2)2]B(C₆H₅)4 

Relevant academic research and scientific papers

KINETICS OF THE REACTION OF 2-(2,4-DINITROPHENOXY)-N-ETHYLPYRIDINIUM TETRAPHENYLBORATE WITH AROMATIC AMINES IN ACETONITRILE

The reactions of 2-(2,4-dinitrophenoxy)-N-ethylpyridinium salts with arylamines take place by nucleophilic substitution at a carbon atom of the benzene ring with the formation of 2,4-dinitrodiphenylamine derivatives.The sensitivity coefficient (ρ0) to the induction effect of the substituents in the arylamine does not depend on the temperature in the range of 10-55 deg C and is equal to -6.89.The constant of the leaving group (τAr) for the 2-hydroxy-N-ethylpyridinium cation amounts to 1.66.