959-68-2

Usage

Yellow solid

Indicates the physical appearance of the compound.

Used in the synthesis of pharmaceuticals and dyes

Indicates the compound's practical applications in the production of medications and coloring agents.

Belongs to the class of imines and phenols

Indicates the compound's chemical classification and structure.

Strong absorption of ultraviolet light

Indicates the compound's ability to absorb UV light, which can be useful in various applications.

Used as a reactant in organic synthesis

Indicates the compound's reactivity and its use in creating other chemical compounds.

Potential biological and pharmacological activities

Indicates that the compound has been studied for its possible effects on living organisms and its potential therapeutic uses.

Antioxidant and antimicrobial properties

Indicates the compound's ability to reduce oxidative stress and inhibit the growth of microorganisms.

Toxic if ingested, inhaled, or in contact with the skin

Indicates the compound's potential health hazards and the need for proper handling and safety precautions.

May cause skin and eye irritation

Indicates the compound's potential to cause adverse effects on the skin and eyes, and the need for appropriate protective measures.

InChI:InChI=1/C13H10N2O3/c16-13-7-2-1-4-10(13)9-14-11-5-3-6-12(8-11)15(17)18/h1-9,14H

Upstream product

• 90-02-8 salicylaldehyde 
• 99-09-2 3-nitro-aniline 
• 89-95-2 2-methyl-benzyl alcohol 

Downstream Products

• 104986-79-0 SnBr₂((HO)C₆H₄CHNC₆H₄(NO₂))2 
• 86322-56-7 UO₂(HOC₆H₄CHNC₆H₄NO₂)2(NO₃)2 
• 75133-42-5 SbCl₃(C₆H₄(OH)CHNC₆H₄NO₂) 
• 75133-48-1 SbCl₅(C₆H₄(OH)CHNC₆H₄NO₂) 
• 104956-95-8 Sn(NCS)2((HO)C₆H₄CHNC₆H₄(NO₂))2 
• 226217-93-2 bis[2-(3-nitrophenylnitrilomethylidyne)phenolato-N,O]zinc(II) 
• 62661-41-0 VO(OC₆H₄CHN(C₆H₄NO₂))2 
• 1182712-23-7 [Cr(salicylidene-3-nitroaniline(-1H))2(H₂O)2]Cl 
• 1092685-87-4 Na(salicylidene-3-nitro-1-aminobenzene-H) 
• 126884-72-8 (2,3-Dihydro-benzofuran-3-yl)-(3-nitro-phenyl)-amine 
• 99779-32-5 2-chloro-N-(2-hydroxybenzyl)-N-(3-nitrophenyl)acetamide 
• 99779-36-9 4-(3-nitrophenyl)-4,5-dihydrobenzo[f][1,4]oxazepin-3(2H)-one 
• 1222170-31-1 4-(3-nitrophenyl)-4,5-dihydrobenzo[f][1,4]oxazepin-3(2H)-thione 
• 99779-37-0 2-((3-nitrophenylamino)methyl)phenol 

Relevant academic research and scientific papers

Antimony(III) and bismuth(III) complexes containing O- and N-chelating ligands: Synthesis, FT-IR, 1H and 13C NMR spectroscopic and mass spectrometric studies

Reaction of SbCl3 with sodium salt of vanillinidene-2-methylaminobenzene (vmabH) and salicylidene-3-nitroaminobenzene (snabH) in 1:1 and 1:2 molar ratios afforded complexes of the type [Sb(η2-sb)nCl3-n ](1-4) [w

Chitosan supported Zn(II) mixed ligand complexes as heterogeneous catalysts for one-pot synthesis of amides from ketones via Beckmann rearrangement

Chitosan supported Zn(II) mixed ligand complexes have been synthesized and characterized by FT-IR, UV–Vis, TGA, XRD, FESEM, EDX, AAS and Elemental Analysis. These complexes have been found to be efficient and recyclable heterogeneous catalysts for the one-pot synthesis of amides via Beckmann rearrangement. All three complexes can be easily filtered out from the reaction medium and reused up to five times without significant loss of catalytic activity. The reported protocol is economical and novel in the sense that amides can be easily synthesized in only one-step. All products were obtained as white to off-white crystalline solids and fully characterized by 1H NMR, FT-IR and Mass Spectra.

Synthesis and development of Chitosan anchored copper(II) Schiff base complexes as heterogeneous catalysts for N-arylation of amines

Abstract The Chitosan anchored Cu(II) Schiff base complexes (C1-C3) have been synthesized and characterized by FTIR, UV, FE-SEM, EDAX, TGA, AAS and elemental analysis. These complexes have been found to be efficient and recyclable heterogeneous catalysts for the Chan-Lam C-N coupling reaction of various aromatic/aliphatic amines with arylboronic acid under mild reaction conditions. These complexes can be easily filtered out from the reaction medium and reused up to five times without significant loss of catalytic activity.

Synthesis of metal complexes of schiff bases and their nematicidal activity against root knot nematode meloidogyne incognita

Six metal complexes were synthesized from Cd (II), Mn (II) and Zn (II) chloride and ligands 2-((3- nitrophenylimino)methyl)phenol (HL1) and 2-((4-nitrophenylimino)methyl)phenol (HL2) in 1:2 M ratio. Microanalytical data, UV-Visible spectral data, magnetic susceptibility, IR, 1HNMR, 13CNMR, mass and molar conductance measurements were used to characterize the structure of complexes. The complexes were found to be non electrolytic on the basis of molar conductance studies. The Schiff bases and their metal complexes had also been screened for their antinemic activity against root knot nematode, Meloidogyne incognita. Complexes have shown significant antinemic activity than their corresponding Schiff bases.

Triorganotin(IV) derivatives of bidentate schiff bases: Synthesis and spectral studies

Reaction of tri-n-butyl tin(IV) chloride with the sodium salt of Schiff bases [salicylidene-2-aminopyridine (sapH), salicylidene-2-amino-4-picoline (sapicH), salicylidene-2-methyl-1-aminobenzene (o-smabH), salicylidene-4-methyl- 1-aminobenzene (p-smabH),

Synthesis of 2-imino-3-aminobenzofurans via multicomponent reactions from TosMIC

A simple synthesis of 2-imino-3-aminobenzofurans was developed based on multicomponent reactions from p-toluenesulfonylmethylisocyanide, salicylaldehyde, and substituted anilines. The crystal structures of two of the aminobenzofurans were established by X-ray crystal structure analysis.

Synthesis and spectral studies of some new dimeric [(μ-Cl) 2M2(L)2 · xTHF] [M = Zn(II) and Hg(II)] complexes containing Schiff-base ligands

A series of binuclear Schiff-base complexes of zinc(II) and mercury(II) containing bidentate ligands (HL) [HL = salicylidene-2-methyl-1-aminobenzene (HL1), salicylidene-2-aminopyridine (HL2), and salicylidene-3-nitro-1-aminobenzene (

Synthesis and physicochemical characterization of some hexacoordinated tin(IV) Schiff base complexes

A freshly distilled tin(IV) tetrachloride interacted with sodium salts of Schiff bases in 1:2 molar ratios in a mixture of tetrahydrofuron (THF)-C 6 H6 produced complexes of the type [SnCl2 (sb) 2 ], [where sb =

Synthesis, spectroscopic (IR, electronic, FAB-mass, and PXRD), magnetic, and antimicrobial studies of new iron(III) complexes containing Schiff bases and substituted benzoxazole ligands

Mixed ligand complexes of iron(III), [Fe(sb)2(py)Cl] 2H 2O (1-9) [where sbH = Schiff bases (derived from condensation of 2-aminopyridine (sapH), 2-aminophenol (saphH), o-toluidine (o-smabH), aminobenzene (sabH), p-toluidine (p-smabH), 3-nitroaniline (snabH), and anthranilic acid (saaH) with salicylaldehyde and substituted (mercapto-)benzimidazole (mbzH), {2-(o-hydroxyphenyl)}benzoxazole, (pboxH)], have been synthesized by the interactions of iron(III) chloride with corresponding ligands in 1 : 2 molar ratio in refluxing pyridine. These complexes have been characterized by elemental analyses, melting points, spectral, and magnetic studies. Powder X-ray diffraction studies of some representative complexes are also reported herein. The antibacterial and antifungal activities of the free ligands and their iron(III) complexes were found invitro. The complexes showed good antibacterial and antifungal effect to some bacteria and fungi. Two standard antibiotics (chloromphenicol and terbinafine) were used for comparison with these complexes.

Synthesis, spectroscopic (IR, electronic and FAB-mass) and magnetic studies of some mixed ligand complexes of chromium (III)

Some new mixed ligand complexes of chromium (III) of the type [Cr(L) 2(L1)Cl].2H2O [where LH = Schiff bases (derived from the condensation of 2-aminopyridine, 2-aminophenol, o-toludine, p-toludine, aniline, 3-nitroaniline and anthranilic acid with salicylaldehyde/vanillin and substituted benzimidazole/benzoxazole, or mercaptobenzimidazole; L=pyridine] have been synthesized by the interactions of chromium (III) chloride with corresponding ligand in 1:2 molar ratio in refluxing pyridine solution. The resulting products have been characterized by elemental analysis and spectral as well as magnetic susceptibility measurements. Structures of the chromium (III) complexes are also proposed.