80564-13-2

Upstream product

• 117-21-5 3-chlorophthalic anhydride 
• 106-47-8 4-chloro-aniline 

Downstream Products

• 80564-35-8 (Z)-4,4'-Dichloro-2,2'-bis-(4-chloro-phenyl)-[1,1']biisoindolylidene-3,3'-dione 
• 80564-33-6 2-(p-chlorphenyl)-1-(o-tolylimino)-4-chloro-3-thioisoindoline 
• 80564-29-0 2-(p-chlorophenyl)-1-(p-tolylimino)-4-chloro-3-oxoisoindoline 
• 80564-28-9 2-(p-chlorophenyl)-1-(p-tolylimino)-4-chloro-3-oxoisoindoline 
• 80564-22-3 2-(p-chlorophenyl)-4-chloro-1,3-dithiophthalimide 
• 80564-17-6 2-(p-chlorophenyl)-4-chloro-1-thiophthalimide 

Relevant academic research and scientific papers

Efficient synthesis of aryl hydroxylactams by reducing imides with activated zinc dust

A series of aryl hydroxylactams (2a, 2b, 2d-2g, 2i-2k, 2m, and 2n) was synthesized by partially reducing aryl cyclic imides in moderate to excellent yields with activated zinc dust alone in acetic acid. This method was regiospecific and can be employed as an alternative for reported methods to partially reduce aryl cyclic imides. Copyright Taylor & Francis Group, LLC.

Monothio- and Dithio-phthalimides: Part V - Synthesis of Chlorinated β-Isoindigo and Dithio-β-isoindigo Derivatives

The reaction of chlorinated monothio- and dithio-phthalimides (II and III) with amines in equimolar amounts in acetic acid gives 2-aryl-1-arylimino-4-chloro-3-oxoisoindolines (IV) and 2-aryl-1-arylimino-4-chloro-3-thioisoindolines (V), respectively.Compou