278806-95-4

Upstream product

• 1192546-07-8 9-(4-sulfophenylamino)acridine-4-carboxylic acid 
• 150-13-0 4-amino-benzoic acid 
• 108-00-9 N,N-dimethylethylenediamine 
• 62-53-3 aniline 
• 100-46-9 benzylamine 
• 87-59-2 2,3-Dimethylaniline 
• 1192546-08-9 9-(4-carboxyphenylamino)acridine-4-carboxylic acid 
• 371-40-4 4-fluoroaniline 
• 121-57-3 4-aminobenzene sulfonic acid 
• 24782-64-7 9-Oxoacridan-4-carboxylic acid 
• 118-91-2 ortho-chlorobenzoic acid 
• 118-92-3 anthranilic acid 
• 278806-94-3 iso-propyl-9-anilinoacridine-4-carboxylate 
• 278807-00-4 9-oxo-9,10-dihydro-acridine-4-carboxylic acid isopropyl ester 

Downstream Products

• 278806-96-5 N-hydroxysuccinimidyl-9-anilinoacridine-4-carboxylate 
• 1192546-12-5 C₂₁H₁₆N₂O₂ 
• 1192546-09-0 9-(2,3-dimethylphenylamino)acridine-4-carboxylic acid 
• 1192546-07-8 9-(4-sulfophenylamino)acridine-4-carboxylic acid 
• 1192546-08-9 9-(4-carboxyphenylamino)acridine-4-carboxylic acid 

Relevant academic research and scientific papers

9-Amino acridines undergo reversible amine exchange reactions in water: Implications on their mechanism of action in vivo

9-Amino substituted acridities undergo a reversible amine exchange reaction In water under near-physiological conditions via an unstable hemiaminal intermediate. This thermodynamically controlled reaction may have Implications In understanding the mode of

Solid-phase synthesis of acridine-peptide conjugates and their analysis by tandem mass spectrometry

(Matrix presented) A novel and high-yielding synthesis of 9-anilinoacridine-4-carboxylic acid is reported. This acid has been used in the solid-phase synthesis of a small combinatorial library of acridine-peptide conjugates. Tandem mass spectrometry (ES-M