3246-73-9

Usage

Type of compound

Phenolic compound with an imine functional group and a tolyl substituent

Usage

Widely used in the production of dyes, pharmaceuticals, and other industrial products

Properties

Known for its antimicrobial and antioxidant properties

Commercial value

A valuable ingredient in various commercial products

InChI:InChI=1/C14H13NO/c1-11-6-2-4-8-13(11)15-10-12-7-3-5-9-14(12)16/h2-10,15H,1H3

Upstream product

• 90-02-8 salicylaldehyde 
• 95-53-4 o-toluidine 
• 89-95-2 2-methyl-benzyl alcohol 
• 28752-82-1 2-(allyloxy)benzaldehyde 
• 1354644-23-7 N-(2-allyloxybenzylidene)-2-methylbenzenamine 

Downstream Products

• 90-02-8 salicylaldehyde 
• 95-53-4 o-toluidine 
• 89-95-2 2-methyl-benzyl alcohol 
• 96500-60-6 N-o-tolylsalicylaldiminatocarbonyltriphenylphosphinerhodium(I) 
• 91709-37-4 [InCl(OC₆H₄CHNC₆H₄CH₃)2]2 
• 91709-36-3 [InCl₂(OC₆H₄CHNC₆H₄CH₃)]2 
• 90423-00-0 Nb(OCH(CH₃)2)2(OC₆H₄CHNC₆H₄CH₃)3 
• 90442-48-1 Nb(OCH(CH₃)2)3(OC₆H₄CHNC₆H₄CH₃)2 
• 62630-81-3 Ta(OCH(CH₃)2)3(C₁₄H₁₂NO)2 
• 111994-08-2 Ta(OCH(CH₃)2)2(C₁₄H₁₂NO)3 
• 62703-77-9 Ta(OCH(CH₃)2)4(C₁₄H₁₂NO) 
• 68868-44-0 (N-o-tolylsalicylideneiminato)(1,5-cyclooctadiene)iridium(I) 
• 82056-89-1 MoOCl₃(OHC₆H₄CHNC₆H₄CH₃)2 
• 84975-20-2 MoCl₂(CH₃C₆H₄NCHC₆H₄O)2 

Relevant academic research and scientific papers

Extraction behavior of copper(II) with salicylidene aniline and salicylidene toluidine isomers in chloroform from sulfate medium

The solvent extraction of copper(II) from aqueous sulfate solutions was studied using salicylideneaniline and the three isomeric salicylidenetoluidine diluted with chloroform at 25°C. The molecules of these extractants are studied theoretically using ab i

Synthesis, spectroscopic characterization, DFT calculations, and antimicrobial activities of N-arylsalicylaldiminate derivatives of diorganotin(IV)

Equimolar reaction of di-n-butyltin(IV) complexes of bidentate Schiff bases of the type [(n-Bu)2Sn(sb)Cl] with sodium salt of mono-functional bidentate ligands in THF-benzene solution afforded structurally interesting complexes of the type [(n-

ELECTROLUMINESCENT DEVICE USING AZOMETHINE-LITHIUM-COMPLEX AS ELECTRON INJECTION LAYER

In OLEDs, improved efficiency is obtained by compounds which can form inter alia electron injection layers of the formula (I) wherein R1 is a 1-5 ring aryl (including polycyclic), aralkyl or heteroaryl group which is optionally substituted with one or mor

Palladium-Catalyzed Regioselective C-Benzylation via a Rearrangement Reaction: Access to Benzyl-Substituted Anilines

An unprecedented C-benzylation rearrangement reaction, catalyzed by palladium, is reported. The reaction proceeds by rearrangement leading to the direct synthesis of para or ortho benzyl-substituted N-methylanilines. The product is obtained in high regioselectivity, without the need to use a ligand for the catalytic process.

Synthesis, characterization and antimicrobial activity of copper(II) complexes of some ortho-substituted aniline schiff bases; Crystal structure of Bis(2-methoxy-6-imino)methylphenol copper(II) complex

This study presents the synthesis, characterization and antimicrobial activity of copper(II) complexes of some ortho-substituted aniline Schiff bases (L1-L8). The Schiff bases and their respective copper(II) complexes were characteri

Electrocatalytic measurement of H2O2 concentration using bis(N-2-methylphenyl alicyldenaminato)copper(II) spiked in a carbon paste electrode

The electrochemical behavior of a bis(N-2-methylphenyl-salicyldenaminato) copper(II) complex spiked in a carbon paste electrode (BMPSCu-CPE) and its electrocatalytic reduction of H2O2 were examined using cyclic voltammetry, chronoamp

Synthesis, spectroscopic characterization and DNA cleavage studies of dibutyltin(IV) complexes of bidentate Schiff bases

Reactions of di-n-butyltin(IV)dichloride with sodium salts of Schiff bases in tetrahydrofuran-benzene solution in 1:1 and 1:2 stoichiometry afforded complexes of the types [(n-Bu)2Sn(sb)Cl] and [(n-Bu) 2Sn(sb)2], respectiv

Synthesis, reactions, physicochemical characterization and biological studies of titanium(IV) Schiff base complexes

Some titanium(IV) complexes of the type [Ti(Cl)4-n(L) n] (1-2), [where n = 1 or 2, L = Schiff bases; salicylidene-2-methy- 1-aminobenzene (LH)] have been synthesized by the reactions of titanium(IV) chloride with sodium salts of Schi

Gas-phase generation and cyclisation reactions of imidoyl radicals

Some 1,2-diarylimidoyl radicals were generated in the gas-phase by intramolecular radical translocation from ortho-imino-aryloxyl radicals, in turn generated under flash vacuum pyrolysis (FVP) conditions. The imidoyls reacted with XR ortho′-substituents in the N-aryl group to give (in most cases) modest yields of cyclisation products. Depending on the nature of the bridging atom (X), the formation of these products was initiated either by a further hydrogen atom translocation (X = CH2), or by ipso-attack onto the aryl group (R = Ph), or by direct substitution at the heteroatom (X = S). With XR = N(Me)Ph, the major reaction product was probably the result of a competing pathway not involving the corresponding imidoyl.