32386-95-1

Upstream product

• 1875-48-5 N-aminophthalamide 
• 100-52-7 benzaldehyde 

Downstream Products

• 5004-45-5 4-phenyl-2H-phthalazin-1-one 
• 1390649-45-2 2-((benzylidenehydrazono)(phenyl)methyl)benzophenone 
• 1390649-47-4 2-((benzylidenehydrazono)(2,4-dimethylphenyl)methyl)-4',6'-dimethylbenzophenone 
• 1390649-48-5 2-((benzylidenehydrazono)(p-methoxyphenyl)methyl)-4'-methoxybenzophenone 
• 1390649-49-6 2-((benzylidenehydrazono)(p-bromophenyl)methyl)-4'-bromobenzophenone 
• 614-31-3 N-benzyl-N-phenylhydrazine 
• 530740-37-5 2-(N-benzyl-anilino)-isoindoline-1,3-dione 
• 643752-17-4 acetic acid 2-(benzyl-methyl-amino)-3-oxo-2,3-dihydro-1H-isoindol-1-yl ester 
• 643752-18-5 acetic acid 2-benzylamino-3-oxo-2,3-dihydro-1H-isoindol-1-yl ester 
• 643752-10-7 2-[benzyl(methyl)amino]-3-hydroxy-2,3-dihydro-1H-isoindol-1-one 
• 643752-13-0 2-(benzylamino)-3-hydroxy-2,3-dihydro-1H-isoindol-1-one 
• 643752-05-0 2-(benzyl-methyl-amino)-isoindole-1,3-dione 

Relevant academic research and scientific papers

Extending the Scope of the B(C6F5)3-Catalyzed C=N Bond Reduction: Hydrogenation of Oxime Ethers and Hydrazones

The B(C6F5)3-catalyzed hydrogenation is applied to aldoxime triisopropylsilyl ethers and hydrazones bearing an easily removable phthaloyl protective group. The C=N reduction of aldehyde-derived substrates (oxime ethers and hydrazones) is enabled by using 1,4-dioxane as the solvent known to participate as the Lewis-basic component in FLP-type heterolytic dihydrogen splitting. More basic ketone-derived hydrazones act as Lewis bases themselves in the FLP-type dihydrogen activation and are therefore successfully hydrogenated in nondonating toluene. The difference in reactivity between aldehyde- and ketone-derived substrates is also reflected in the required catalyst loading and dihydrogen pressure.

N-aminophthalimide as a synthon for heterocyclic schiff bases: Efficient utilization as corrosion inhibitors of mild steel in 0.5 mol.L-1 H2SO4 solution

MANY Schiff bases were prepared to inhibit the corrosion reactions of mild steel in acidic medium. Their chemical structures were determined by using different techniques. Thermodynamic adsorption parameters of inhibitors were determined using the Langmui

A convenient synthesis of 1-alkyl-1-phenylhydrazines from N-aminophthalimide

N-Alkylaminophthalimides were synthesized by condensation of N-aminophthalimide with aldehydes, and subsequent reduction of the intermediate with pyridine-borane in acetic acid. N-Phenylation and removal of the phthalimide group gave 1-alkyl-1-phenylhydrazines in high yield.

Regioselective Reduction of 2-(Arylideneamino)isoindole-1,3-diones - Synthesis of Alkaloid Analogues by N-Acylhydrazonium Ion Aromatic π-Cyclization

Hydroxylactams 6a-c and 7a-c were synthesized by successive regioselective reductions of arylideneaminophthalimides 3a-c, which were easily available from aminophthalimide 1 and benzaldehyde (2a) or thiophenecarboxaldehydes 2b and 2c. N-Acylhydrazonium io