80241-83-4

Usage

Molecular structure

A complex organic compound consisting of a phenol ring, an attached amino group, and a methylidene bridge.

Substituents

Contains two methoxy groups attached to the phenol ring, contributing to its unique properties.

Stereochemistry

The compound has a (3,4-dimethoxyphenyl)methylidene group, indicating the presence of an E (cis) configuration in its structure.

Potential applications

Due to its unique structure and potential biological activities, 2-[(E)-(3,4-dimethoxyphenyl)methylidene]aminophenol may have applications in the fields of organic chemistry and pharmaceuticals.

Research and testing

Further research and testing are required to fully understand the properties and potential uses of 2-{[(E)-(3,4-dimethoxyphenyl)methylidene]amino}phenol, as its complex structure may lead to novel applications and effects.

Upstream product

• 120-14-9 3,4-dimethoxy-benzaldehyde 
• 95-55-6 2-amino-phenol 

Downstream Products

• 92552-99-3 2-(3,4-dimethoxyphenyl)-1,3-benzoxazole 
• 119577-85-4 N₂-(3,4-dimethoxybenzylidene)aminophenol uranyl nitrate 
• 212578-55-7 2-[4-(3,4-Dimethoxy-benzyl)-3,4-dihydro-2H-benzo[1,4]oxazin-2-yl]-N-[2-(3,4-dimethoxy-phenyl)-ethyl]-acetamide 
• 212578-48-8 [4-(3,4-Dimethoxy-benzyl)-3,4-dihydro-2H-benzo[1,4]oxazin-2-yl]-acetic acid ethyl ester 
• 212578-51-3 [4-(3,4-Dimethoxy-benzyl)-3,4-dihydro-2H-benzo[1,4]oxazin-2-yl]-acetic acid 
• 212578-70-6 2-(3,4-Dimethoxy-benzylamino)-phenol 

Relevant academic research and scientific papers

The electronic structure, solvatochromism, and electric dipole moments of new Schiff base derivatives using absorbance and fluorescence spectra

The electronic structure and electronic transitions of four new mono Schiff base derivatives are interpreted by using absorption and fluorescence spectra including 28 different solution medium. Electrical dipole moments have been found by means of four di

OMS-2/H2O2/Dimethyl Carbonate: An Environmentally-Friendly Heterogeneous Catalytic System for the Oxidative Synthesis of Benzoxazoles at Room Temperature

A manganese octahedral molecular sieve (OMS-2) was found to be an efficient and recyclable heterogeneous catalyst for the oxidative synthesis of benzoxazoles in the gram-scale from phenolic imines at room temperature. H2O2 and biobased reagent dimethyl carbonate (DMC) were successfully employed as the environmentally friendly oxidant and solvent, respectively, in an OMS-2-catalysted redox reaction for the first time. Benzoxazoles could also be obtained from N-substituted 2-aminophenols via Cu(OH)x/OMS-2-catalyzed sequential oxidative transformation at elevated temperatures.

Studies on DNA binding, electrochemical activation, DNA photocleavage, and biopotency of N and O donor bidentate ligands with Cu(II), Co(II), and Zn(II)

Three Schiff-base ligands, namely 2-(3,4-dimethoxybenzylideneamino)phenol (HL1), 2-(3-hydroxy-4-nitrobenzylidene-amino)phenol (HL2), and 2-(3-methoxy-4-hydroxy-benzylideneamino)phenol (HL3) and their Cu(II), Co(II), and Zn

New substituted 1,4-benzoxazine derivatives with potential intracellular calcium activity

Substituted 1,4-benzoxazines bearing an amino side chain at the 2- position were prepared and were found to have a moderate activity on intracellular calcium. Of the compounds studied it was found that those which possess a homoveratrylamino moiety exhibi

Uranyl Nitrate Complexes of Some Schiff Bases Derived from Substituted Benzaldehydes and Amino Compounds

Complexes of uranyl nitrate with ten schiff bases have been prepared and characterised on the basis of analytical, conductance, molecular weight and spectral data.The schiff bases used are; N-(3-methoxy-4-hydroxybenzylidene)benzhydrazone (MHBBH), N-(3-met