3117-61-1

Usage

Uses

Used in Pharmaceutical Industry:
N-Salicylideneamine is used as a building block for the synthesis of various pharmaceutical compounds. Its unique structure allows for the creation of a wide range of molecules with different biological activities, making it a valuable asset in drug discovery and development.
Used in Chemical Synthesis:
N-Salicylideneamine serves as an important intermediate in the synthesis of various organic compounds, including dyes, pigments, and other specialty chemicals. Its reactivity and versatility make it a popular choice for researchers and chemists working in the field of organic synthesis.
Used in Material Science:
Due to its structural properties, N-Salicylideneamine can be utilized in the development of new materials with specific properties, such as conductivity, magnetism, or optical characteristics. It can be incorporated into polymers, nanoparticles, or other advanced materials to enhance their performance and functionality.
Used in Analytical Chemistry:
N-Salicylideneamine can be employed as a reagent or a colorimetric indicator in various analytical techniques. Its ability to form complexes with different metal ions makes it useful for the detection and quantification of specific elements in chemical analysis.

InChI:InChI=1/C7H7NO/c8-5-6-3-1-2-4-7(6)9/h1-5H,8H2/b6-5-

Upstream product

• 90-02-8 salicylaldehyde 
• 38929-70-3 [Ni(OC₆H₄CHNC₆H₅)2] 

Downstream Products

• 215367-19-4 salicylaldiminepropyltriethoxysilane 
• 14220-45-2 bis(N-salicylaldimino) Co(II) 

Relevant academic research and scientific papers

Variability of the Transformations of 4-Hydroxy-6-methyl-2H-pyran-2-one under Modified Biginelli Reaction Conditions

A modified version of the three-component Biginelli reaction of 4-hydroxy-6-methyl-2H-pyran-2-one with aromatic aldehydes in urea under conventional heating and microwave activation has been studied. Depending on the order of addition of the reactants, su

Hydrophobic effect of silica functionalized with silylated Ti-salicylaldimine complex on limonene oxidation by aqueous hydrogen peroxide

This research work describes the effect of hydrophobicity in inducing the diffusion of alkene substrates to the catalytic active sites. The aim of this research is to improve the catalytic activity by tailoring the degree of hydrophobicity of the catalyst. Silica functionalized with solid non-silylated Ti-salicylaldimine complex was prepared at room temperature by mixing imine ligand and Ti(IV) sulphate solution. The amorphous, solid complex formed was further silylated with octadecyltrimethoxysilane (OTMS) to induce hydrophobicity. The composition of the resulting silica functionalized with silylated Ti-salicylaldimine complex was varied with Ti:OTMS molar ratio in the range of 1:1/4 to 1:4 at room temperature. The successful attachment of alkylsilyl groups to silica functionalized with Ti-salicylaldimine complex was proven by the FTIR and 29Si solid state NMR spectra. The FTIR spectra showed increasing peak area for sp 3 C-H stretching mode (ca. 2919 cm-1 and 2850 cm-1) and decreasing peak area for Si-OH band with increasing amount of OTMS. TGA showed less water content with higher amount of alkylsilyl groups in the catalyst. This is in agreement with the lower kinetic rate of water adsorption capacity for the hydrophobic catalysts prepared. It was observed that the hydrophobic, silica functionalized with silylated Ti-salicylaldimine complex exhibited higher substrate conversion and reusability compared to the non-silylated catalyst.

Time-resolved E.S.R. Study of Triplet Ketoamines Generated by Intramolecular Proton Transfer in Free Schiff Bases

Non-phosphorescent triplet states of the ketoamine forms of several free Schiff bases generated by intramolecular proton transfer have been observed using a time-resolved e.s.r. method.

Mixed Tri- and Bi-dentate Schiff-base Complexes of Technetium(V) and Rhenium(V). The Crystal Structure of N-(2-Oxidophenyl)salicylideneiminato-NOO')oxo(8-quinolinolato-NO)technetium(V)

Six-co-ordinate complexes of technetium(V) and rhenium(V) containing the MO3+ core with tri- and bi-dentate Schiff-base ligands were synthesized and characterized.The complexes with general formula 1)L) 1/sup