858859-74-2

Upstream product

• 1075-62-3 N-(6-aminopyridin-2-yl)acetamide 
• 25165-72-4 N-[6-[[(2,2-dimethyl-4,6-dioxo-1,3-dioxan-5-ylidene)methyl]amino]-2-pyridinyl]acetamide 
• 57773-12-3 N-(5-oxo-5,8-dihydro-1,8-naphthyridin-2-yl)-acetamide 
• 1415405-42-3 N-[5-(4-methoxyphenyl)-1,8-naphthyridin-2-yl]acetamide 
• 2881-83-6 ethyl 4-methoxybenzoylacetate 
• 141-86-6 2.6-diaminopyridine 
• 858859-62-8 N-[5-(4-methoxy-phenyl)-7-oxo-7,8-dihydro-[1,8]naphthyridin-2-yl]-acetamide 
• 858859-61-7 7-amino-4-(4-methoxy-phenyl)-1H-[1,8]naphthyridin-2-one 
• 858859-64-0 7-chloro-5-(4-methoxy-phenyl)-[1,8]naphthyridin-2-ylamine 

Downstream Products

• 858859-76-4 5-{4-[2-(3,5-di-tert-butyl-phenyl)-ethoxy]-phenyl}-[1,8]naphthyridin-2-ylamine 
• 858859-75-3 4-(7-amino-[1,8]naphthyridin-4-yl)-phenol 

Relevant academic research and scientific papers

Synthesis of 1,8-naphthyridines and their application in the development of anionic fluorogenic chemosensors

Two 1,8-naphthyridines were synthesized and found to be fluorescent in solution. These compounds were studied in the presence of Cu+ and Cu2+ ions and it was verified that the metal causes the quenching of their fluorescence emission

Synthesis of a soluble ureido-naphthyridine oligomer that self-associates via eight contiguous hydrogen bonds

(Chemical Equation Presented) An iterative synthetic route to organic-soluble ureido-naphthyridine oligomers has been developed. Use of this protocol allowed synthesis of a short ureido-naphthyridine oligomer, which presents a self-complementary DDAADDAA hydrogen bonding array (D = hydrogen bond donor, A = hydrogen bond acceptor). Strong self-association via eight hydrogen bonds was observed in organic solution.