94136-57-9

Upstream product

• 58885-60-2 N-(tert-butoxycarbonyl)-3-aminopropanal 
• 622-33-3 N-benzyloxyamine 
• 2687-43-6 O-benzylhydoxylamine hydrochloride 
• 58885-58-8 N-tert-butoxycarbonyl-3-aminopropanol 
• 24424-99-5 di-tert-butyl dicarbonate 

Downstream Products

• 83948-50-9 1-<(tert-Butoxycarbonyl)amino>-3-propane 
• 94136-74-0 N,N'-bis<3-propyl>-2,6-pyridinedicarbamide 
• 84627-28-1 dichlorhydrate de 1-amino-3-(benzyloxyamino)propane 
• 83948-61-2 1-Amino-3-propane Hydrochloride 
• 132149-24-7 N,N'-bis<3-(acetylbenzyloxyamino)propyl>-<4-(3-nitrilepropyloxy)-2,6-pyridine>dicarbamide 
• 132149-18-9 trifluoroacetate de 1-amino-3-(acetylbenzyloxyamino)propane 
• 132149-20-3 N,N'-bis<3-(acetylbenzyloxyamino)propyl>-<4-pentoxy-2,6-pyridine>dicarbamide 
• 132149-23-6 N,N'-bis<3-(acetylbenzyloxyamino)propyl>-<4-ethoxy-2,6-pyridine>dicarbamide 
• 83948-64-5 1-Amino-3-<(benzyloxy)amino>propane p-Toluenesulfonic Acid Double Salt 
• 94136-58-0 1-<(tert-butoxycarbonyl)amino>-3-<(benzyloxy)amino>propane 

Relevant academic research and scientific papers

THE DESIGN OF MAGNETIC RESONANCE CONTRAST AGENTS: NEW IRON (III) DIHYDROXAMATE COMPLEXES

We have prepared a series of dihydroxamates and their iron(III) complexes in view of obtaining new NMR imaging agents.Four new dihydroxamic acid ligands have been synthesized by condensation of 4-substituted-2,6-pyridine dicarboxylic acids with N-aminopro