877869-03-9

Upstream product

• 754216-33-6 4-isobutoxy-8-nitro-2-quinolinecarboxylic acid chloride 
• 620169-94-0 4-isobutoxy-8-nitro-2-quinoline-2-carboxylic acid 
• 517883-19-1 methyl 4-isobutoxyl-8-nitroquinoline-2-carboxylate 
• 877869-02-8 4-isobutoxy-8-nitroquinoline-2-carboxylic acid phenylamide 

Downstream Products

• 877869-14-2 C₆₂H₆₃N₉O₈ 
• 1005329-65-6 9-{2-[(4,7-diisobutoxy-9-phenylcarbamoyl-[1,10]phenanthroline-2-carbonyl)-amino]-phenylcarbamoyl}-4,7-diisobutoxy-[1,10]phenanthroline-2-carboxylic acid 
• 877869-13-1 9-{2-[(4,7-diisobutoxy-9-phenylcarbamoyl-[1,10]phenanthroline-2-carbonyl)-amino]-phenylcarbamoyl}-4,7-diisobutoxy-[1,10]phenanthroline-2-carboxylic acid methyl ester 
• 877869-08-4 4,7-diisobutoxy-[1,10]phenanthroline-2,9-dicarboxylic acid 2-[(2-amino-phenyl)-amide] 9-phenylamide 
• 877869-07-3 4,7-diisobutoxy-9-phenylcarbamoyl-[1,10]phenanthroline-2-carboxylic acid 
• 877869-06-2 4,7-diisobutoxy-9-phenylcarbamoyl-[1,10]phenanthroline-2-carboxylic acid methyl ester 
• 877869-05-1 7-isobutoxy-4-oxo-9-phenylcarbamoyl-1,4-dihydro-[1,10]phenanthroline-2-carboxylic acid methyl ester 

Relevant academic research and scientific papers

Anion receptors based on a quinoline backbone

2-Amido-8-urea substituted quinoline derivatives are potent receptors for the binding of halide or benzoate anions in chloroform. The selectivity and affinity of the receptors for fluoride can be tuned by variation of the substituents at the receptor side

Phenanthroline dicarboxamide-based helical foldamers: Stable helical structures in methanol

A series of new aromatic oligoamides 2-5 based on 1,10-phenanthroline diacid and o-phenylenediamine have been synthesized through a convergent segment coupling strategy. These oligomers can fold into well-defined helical structures in solution through int