88914-97-0

Upstream product

• 32305-23-0 N-(2-Methoxyphenyl)-4-chloroanthranilic acid 
• 50-84-0 2,4 dichlorobenzoic acid 
• 90-04-0 2-methoxy-phenylamine 

Downstream Products

• 108835-78-5 [4-(3-Chloro-5-methoxy-acridin-9-ylamino)-3-methylamino-phenyl]-carbamic acid methyl ester 
• 106521-42-0 N-[4-(3-Chloro-5-methoxy-acridin-9-ylamino)-3-dimethylamino-phenyl]-methanesulfonamide; hydrochloride 
• 94551-42-5 3-chloro-5-methoxy-9-phenoxy-acridine 
• 1610849-77-8 6-chloro-4-methoxy-9-(2-aminoanilino)acridine hydrochloride 
• 112767-39-2 (3-Chloro-5-methoxy-acridin-9-ylsulfanyl)-acetic acid; compound with morpholine 
• 112759-12-3 (3-Chloro-5-methoxy-acridin-9-ylsulfanyl)-acetic acid; compound with piperidine 
• 102941-21-9 N-[4-(3-Chloro-5-methoxy-acridin-9-ylamino)-3-methylamino-phenyl]-methanesulfonamide; hydrochloride 

Relevant academic research and scientific papers

A rapid, chromatography-free route to substituted acridine-isoalloxazine conjugates under microwave irradiation

Microwave irradiation was applied to a sequence of condensation reactions from readily available 9-chloroacridines to provide a range of novel acridine-isoalloxazine conjugates. The combination of these two moieties, both of biological interest, was achieved by a chromatography-free route.