1624-54-0

Upstream product

• 90-02-8 salicylaldehyde 
• 95-55-6 2-amino-phenol 
• 4846-21-3 O-phenylhydroxylamine 

Downstream Products

• 835-64-3 2-(2-Hydroxyphenyl)benzoxazole 
• 51152-29-5 (Z)-2-((2-hydroxybenzylideneamino)phenol) 
• 1173702-44-7 12-phenoxy-11,13-dioxa-5-aza-12-phospha-dibenzo[a,e]cyclononen-12-oxide 
• 1226778-28-4 [ReBr(PPh₃)2(2-[(2-hydroxyphenyl)iminomethyl]phenol(-2H))] 
• 36282-74-3 2-<(o-hydroxybenzyl)amino>phenol 

Relevant academic research and scientific papers

Supramolecular structures of mononuclear and dinuclear dioxomolybdenum(VI) complexes via hydrogen bonds and π-π Stacking, thermal studies and electrochemical measurements

Two dioxomolybdenum(VI) complexes, [Mo2O4(HBAP) 2L] (1) and [MoO2(HMBI)] (2) (HBAP = ((E)-2-(2- hydroxybenzylidene)amino)phenol, HMBI = ((E)-N′-(2-hydroxy-3- ethoxybenzylidene)isonicotinohydrazide) and L = (4,4′

Synthesis, crystal structure and spectroscopic studies of 2-{(E)-[2-hydroxyphenyl)imino]methyl} phenol schiff base molecule

A new Schiff-base complex 2-{(E)-[2-hydroxyphenyl)imino]methyl}phenol has been synthesized and characterized by elemental analyses, UV-VIS and IR spectroscopy and single crystal X-ray determination. The structure comprises two independent and similar mole

Single-Molecule Magnetism in Dy2 Cluster Based on a Schiff Base Ligand

Two dinuclear LnIII-based clusters, namely [Dy2L2(NO3)2(DME)4] (1) and [Gd2L2(NO3)2(DME)4] (2) [H2L = (E)-2-((2-hydroxybenz

Structural, proton-transfer, thermodynamic and nonlinear optical studies of (E)-2-((2-hydroxyphenyl)iminiomethyl)phenolate

Recently, the study of imine-bridged organics is interested in proton-transfer and photo-responsive material fields. Herein, we make a investigation on the structural, thermodynamic and nonlinear optical properties of (E)-2-((2-hydroxyphenyl)iminiomethyl)

Synthesis, x-ray crystallography, molecular docking and biological screening of 2-aminophenol based Schiff bases

Schiff bases, 2-{[(2-hydroxyphenyl)methylidene]amino}phenol (4) and 2-{[3-4-(dimethylamino)phenyl-2-propenylidene]amino}phenol (5), have been synthesized by the condensation of 2-aminophenol (1) with 2-hydroxybenzaldehyde (2) and 4-dimethylaminocinnamalde

Encrypted optical markers for security applications

Encrypted markers that are not readily detectable can be revealed by treatment with a specific reagent used as a developer to reveal a readily detectable physical property of the marker, such as a characteristic fluorescence emission after excitation with

A family of silatrane-armed triazole-encapped salicylaldehyde-derived Schiff bases: Synthesis, spectral analysis, and antimicrobial and quantum chemical evaluation

This work describes the successful synthesis of salicylaldehyde-derived Schiff base-linked organosilicon compounds following a highly efficient click approach. Hydroxyl-terminated Schiff bases were alkylated to bis-acetylenes (1–3) which upon 3?+?2 cycloaddition with 3-azidopropyltriethoxysilane yielded triazole-decorated bis-silanes (4–6). These silanes further underwent base-catalyzed transesterification to afford Schiff base-linked triazole-bound organosilatranes (7–9). The final silatranes as well as precursor alkynes and silanes were comprehensively characterized using NMR (1H and 13C) and infrared spectroscopic techniques together with elemental analysis and mass spectrometry of compounds 7–9. Also, the structures of alkynes 1–3 and silatrane 7 were validated using single-crystal X-ray crystallography. Organosilatranes were initially screened for their pharmacokinetic profile using absorption, distribution, metabolism, excretion and toxicity (ADMET) tools and then explored for their antimicrobial activities, with compound 9 emerging as the most potent antimicrobial agent. Compounds 1–3 and 7–9 also underwent thorough computational analysis by applying the density functional theory (DFT) approach with B3LYP/6-31G(d) level of theory and the results were found to be consistent with the experimental data. Several DFT-based descriptors were also evaluated providing a valuable insight into molecular stability and reactivity.

Substituent effects on solvent-free epoxidation catalyzed by dioxomolybdenum(VI) complexes supported by ONO Schiff base ligands

Molybdenum complexes of type [MoO2L]n (L = tridentate ONO Schiff base ligands based on the salicylidene-2-aminophenolato structure) have been synthesized and used as catalysts for the solvent-free epoxidation of olefins. The effect o

Design, synthesis and biological evaluation of imine resveratrol derivatives as multi-targeted agents against Alzheimer's disease

A series of imine resveratrol derivatives (1-20) have been designed, synthesized, and evaluated as multi-targeted compounds for the treatment of Alzheimer's disease (AD). In vitro studies show that most of the molecules exhibit a significant ability to in

The antioxidant effect of imine resveratrol analogues

Twenty five Imine resveratrol analogues (IRAs) were synthesized, replacing the CC bond in resveratrol with CN bond, as well as substitution modifications on aromatic rings. Radical scavenging activities against DPPH, along with singlet oxygen quenching capacities were evaluated, and further confirmed using density functional theory calculations (DFT). It was found that IRAs bearing ortho-OH on B ring have better radical scavenging activities against DPPH than resveratrol, these compounds were also found to be effective 1O 2 quenchers. Theoretical studies on the reaction mechanism of these compounds with 1O2 suggest that the 1,3-addition to a double bond with a -OH group with the formation of allylic hydroperoxide is the most probable reaction route.