78174-01-3

Upstream product

• 134-32-7 1-amino-naphthalene 
• 121-33-5 vanillin 

Relevant academic research and scientific papers

Sensing of Fe(III) ion via turn-on fluorescence by fluorescence probes derived from 1-naphthylamine

Fluorescence probes NA1 and NA2 derived from 1-naphthylamine (NA) as fluorophore have been synthesized and characterized by different spectroscopic studies. Identification behaviour of these probes towards various metal ions has been investigated. Both th

Synthesis of Schiff bases from 1-naphthylamine and vanillin, vanillal, and their O-acyl derivatives

Previously unknown Schiff bases were synthesized by the condensation of 1-naphthylamine with vanillin, vanillal, and their O-acyl derivatives in ethanol. Pleiades Publishing, Inc., 2006.

Analgesic, anti-inflammatory activity and docking study of 2-(substituted phenyl)-3-(naphthalen-1-yl)thiazolidin-4-ones

A potential analgesic and anti-inflammatory activities have been reported in 4-thiazolidinone analogs as well as some drugs bearing naphthyl moiety such as naproxen. Thus a reported series of 2-(substituted phenyl)-3-(naphthalen-1-yl)thiazolidin-4-ones (T

Analgesic, anti-inflammatory activity and docking study of 2-(substituted phenyl)-3-(naphthalen- 1-yl)thiazolidin-4-ones

A potential analgesic and anti-inflammatory activities have been reported in 4-thiazolidinone analogs as well as some drugs bearing naphthyl moiety such as naproxen. Thus a reported series of 2-(substituted phenyl)-3-(naphthalen-1-yl)thiazolidin-4- ones (

A study of anti-inflammatory activity of some novel α-amino naphthalene and β-amino naphthalene derivatives

In the present study, some naphthalene derivatives have been synthesized by incorporating azetidinyl and thiazolidinyl moieties at its α- or β-positions such as a-(3-chloro-2-oxo-4-substitute-d)aryl-1-azetidinyl) naphthalenes 6-10, α-((substituted)aryl-4-

Quantitative solid-solid synthesis of azomethines

Twenty preparatively useful azomethines have been quantitatively (100% yield at 100% conversion) obtained as hydrates by grinding together solid anilines with solid benzaldehydes without passing through liquid phases. Unlike (acid catalyzed) azomethine syntheses in solution, the solid-solid condensations proceed 'waste-free'. The solid-state mechanisms have been elucidated by atomic force microscopy (AFM) and in part by scanning near-field optical microscopy (SNOM) in three cases. The results indicate long distance migration of the aldehydes into the lattice of the aniline derivatives. Stumpy protrusions are formed at the direct points of contact but also distance sublimation (100 nm range) is succesful in the case of p-chlorobenzaldehyde and p-nitroaniline. Long-range flow of 4-hydroxybenzaldehyde molecules on its (010)-face into contracting crystals of p-toluidine or p-anisidine occurs along two different cleavage planes. Steep hills and valleys are left behind. The molecular migrations through the sites of contact are interpreted in terms of crystals packing. The ease of these solid-solid condensation reactions relies on the crystal packing.

Spectrophotometric Study of Some Praseodymium(III) Schiff Base Complexes

Schiff base complexes of praseodymium(III) have been synthesized and characterized on the basis of electronic and infrared spectral studies.The gaussian analyses of different absorption bands and application of Judd-Ofelt theory has given the values for v

Synthesis and Characterization of Some Mixed Ligand Complexes of Ni(II) Ethylacetoacetate with Schiff Bases

Some mixed ligand complexes of Ni(II) ethylacetoacetate with Schiff bases are synthesised and characterized by elemental analyses, magnetic, electronic and ir spectral studies.The results indicate that the complexes have near octahedral structure and the ligand is coordinated through nitrogen atom of azomethine group.