Some scientific research about 3-Amino-2-naphthoic acid

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Reactions catalyzed within inorganic and organic materials and at electrochemical interfaces commonly occur at high coverage and in condensed media, causing turnover rates to depend strongly on interfacial structure and composition, 5959-52-4, Name is 3-Amino-2-naphthoic acid, SMILES is NC1=CC2=C(C=CC=C2)C=C1C(O)=O, in an article , author is Huang, Chang-Yao, once mentioned of 5959-52-4, Recommanded Product: 3-Amino-2-naphthoic acid.

Synthesis and Catalytic Activity of Water-Soluble Ruthenium(II) Complexes Bearing a Naphthyridine Carboxylate-Ligand

The synthesis of water-soluble (eta(6)-arene)ruthenium(II) complexes based on pyrazolyl naphthyridine ligands modified with a carboxylate group is reported. The complexes are easily accessible in good yields via complexation of [(arene)RuCl2](2) with 7-pyrazolyl-1,8-naphthyridine-2-carboxylic acid (1). All complexes have been characterized by spectroscopic and elemental analyses. The complexes {[Ru(eta(6)-arene)(N,N’-1)Cl]Cl} (arene = benzene (5), p-cymene (6)) were further confirmed by X-ray diffraction studies. These complexes are soluble in water (ca. 10 mg/mL) and are catalytically active in hydrogen-transfer reduction of carbonyl compounds in aqueous medium with the use of HCOOH/HCOONa as the hydrogen source.

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Reference:
1,8-Naphthyridine – Wikipedia,
,1,8-Naphthyridine | C8H6N2 – PubChem