85468-48-0

Upstream product

• 1445-69-8 2,3-dihydrophthalazine-1,4-dione 
• 123-11-5 4-methoxy-benzaldehyde 
• 1875-48-5 N-aminophthalamide 
• 85-44-9 phthalic anhydride 
• 136918-14-4 phthalimide 
• 4397-55-1 phthalic monoacid monomethyl ester chloride 
• 4388-29-8 [2,2'-biisoindoline]-1,1',3,3'-tetraone 

Downstream Products

• 345928-21-4 2-((4-methoxybenzyl)amino)isoindoline-1,3-dione 
• 104747-14-0 o-Phthalic Acid Monohydrazide p-Methoxybenzal 
• 1773-49-5 (E)-1-(2,4-dinitrophenyl)-2-(4-methoxybenzylidene)hydrazine 
• 1445-69-8 2,3-dihydrophthalazine-1,4-dione 
• 140-69-2 4-methoxybenzylhydrazine 

Relevant academic research and scientific papers

Reactions of N-Aminophthalimide With Electrophiles. II. Preparation and Properties of Araldehyde Hydrazones

N-Aminophthalimide (I) reacted with a variety of aromatic aldehydes to give the related arylideneaminophthalimides (III-X), although typical ketones such as acetone and benzophenone did not under the specific conditions employed.Catalytic reduction of benzylideneaminophthalimide (III) led to N-benzylaminophthalimide (XI), a stable acid-free precursor of benzylhydrazine.

Studies in Antifertility Agents : Part XXXVI-Syntheses of N-(Substituted benzylidene)amino-phthalimides, -dihydroisoindoles and -1,2,3,4-tetrahydroisoquinolines

Syntheses and antifertility activity of a number of N-(substituted benzylidene)amino-phthalimides (3a-i), -dihydroisoindoles (4a-i) and -1,2,3,4-tetrahydroisoquinolines (5a-i) are reported.Some of these compounds prevent pregnancy when administered at 25 mg/kg/day in mice. 100percent abortifacient actvity has been shown by some of these compounds in rats at 20 mg/kg.