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• 150-13-0 4-amino-benzoic acid 
• 708-06-5 2-hydroxynaphthalene-1-carbaldehyde 

Relevant academic research and scientific papers

A highly selective fluorescent chemosensor for Al(III) ions based on 2-hydroxy-1-naphthaldehyde derivative

This manuscript reports the synthesis and fluorescent chemosensor property of a Schiff base derivative, 4-[(2-hydroxy-1-naphthyl) methylideneamino]benzoic acid (H2L). The fluorescence spectrum shows that H2L exhibits a highly selecti

Solvent-free oxidation of ethylbenzene over LDH-hosted Co(II) Schiff base of 2-hydroxy-1-naphthaldehyde and 4-amino benzoic acid

Co(II) Schiff base complexes derived by condensation of 4-amino benzoic and 2-hydroxy-1-naphthaldehyde was immobilized into layered double hydroxide, {LDH-[NAPABA-Co(II)]} and characterized by various techniques namely ICP-AES, SEM, TEM, EDX, XRD, FTIR, BET surface area, EPR, TGA, and DRUV–vis. spectroscopy. The structures of the Co(II) Schiff base complex are optimized by DFT calculations. The catalytic activity of the heterogenized Co(II) Schiff base complex for the oxidation of ethylbenzene using tert-butylhydroperoxide is studied under a solvent-free condition. Ethylbenzene upon oxidation gave benzaldehyde, acetophenone, and benzoic acid with 67.4% conversion of ethylbenzene and 99.57% selectivity of acetophenone. The catalyst is recyclable up to six cycles without notable loss of their activity.

Cu(ii) Schiff base complex intercalated into layered double hydroxide for selective oxidation of ethylbenzene under solvent-free conditions

A new heterogeneous catalyst was prepared by intercalation of NNOO donor Cu(ii) Schiff base complex derived from 2-hydroxy-1-naphthaldehyde and 4-amino benzoic acid into Zn-Al layered double hydroxide {LDH-[NAPABA-Cu(ii)]}. Synthesized catalyst was characterized by Inductively coupled plasma atomic emission spectroscopy, energy dispersive X-ray analysis, scanning electron microscopy, X-ray diffraction, Transmission electron microscopy, BET surface area, Fourier transform infrared spectroscopy, thermo-gravimetric analysis, electron paramagnetic resonance spectroscopy and diffuse reflectance UV-visible spectroscopy. The catalytic performance of LDH-[NAPABA-Cu(ii)] was studied for the liquid phase solvent-free oxidation of ethylbenzene at 393 K, using tert-butylhydroperoxide as an oxidant. In oxidation reaction ethylbenzene was oxidized to acetophenone, benzaldehyde and benzoic acid. The major product was acetophenone. A maximum, 80.54% conversion of ethylbenzene was observed after 7 hours. The catalyst was recycled seven times without significant loss of catalytic activity.

The synthesis of novel methotrexate-like compounds

Methotrexate (MTX) is a folate antagonist used in treatment of several chronic inflammatory and neoplastic conditions. In this study, new MTX-like compounds that may-be potential anticancer agents were synthesized and their structures were determined by IR, UV, GC-MS, 1H NMR, and 13C NMR spectra. Also, in this study, a series structurally related to MTX or folate analogous compounds were evaluated whether they have inhibitory properties on the dihydrofolate reductase activity (DHFR).