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3946-91-6 Usage

Chemical Properties

solid

Check Digit Verification of cas no

The CAS Registry Mumber 3946-91-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,9,4 and 6 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3946-91:
(6*3)+(5*9)+(4*4)+(3*6)+(2*9)+(1*1)=116
116 % 10 = 6
So 3946-91-6 is a valid CAS Registry Number.

3946-91-6 Well-known Company Product Price

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  • TCI America

  • (D2572)  N,N'-Bis(salicylidene)-1,2-phenylenediamine  >96.0%(HPLC)(N)

  • 3946-91-6

  • 5g

  • 680.00CNY

  • Detail
  • TCI America

  • (D2572)  N,N'-Bis(salicylidene)-1,2-phenylenediamine  >96.0%(HPLC)(N)

  • 3946-91-6

  • 25g

  • 1,890.00CNY

  • Detail

3946-91-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N'-DISALICYLAL-1,2-PHENYLENEDIAMINE

1.2 Other means of identification

Product number -
Other names N,N'-bis(salicyclidene)-1,2-phenylenediamine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:3946-91-6 SDS

3946-91-6Relevant articles and documents

Determination of trace uranium by resonance fluorescence method coupled with photo-catalytic technology and dual cloud point extraction

Li, Jiekang,Li, Guirong,Han, Qian

, p. 208 - 215 (2016)

In this paper, two kinds of salophens (Sal) with different solubilities, Sal1 and Sal2, have been respectively synthesized, and they all can combine with uranyl to form stable complexes: [UO2 2?+-Sal1] and [UO2 2?+/s

Synthesis, structural features, antibacterial behaviour and theoretical investigation of two new manganese(III) Schiff base complexes

Paul, Pranajit,Bhowmik, Kanti R.N.,Roy, Subhadip,Deb, Dibakar,Das, Nandita,Bhattacharjee, Maitri,Dutta Purkayastha,Male, Louse,Mckee, Vickie,Pallepogu, Raghavaiah,Maiti, Debasis,Bauza, Antonio,Fontera, Antonio,Kirillov, Alexander M.

, p. 407 - 416 (2018)

Two discrete manganese(III) coordination compounds, [Mn(L)(OCN)]2 (1) and [Mn(L′)(H2O)2][dnba]·DMF·H2O (2) bearing in situ generated Schiff base ligands H2L [H2L = N,N′-o-phenylenebis(salic

Synthesis, Characterization, and Biological Activity of Organotin(IV) Complexes with Schiff Bases

Nazneen,Ali,Shahzadi,Shujah

, p. 2970 - 2978 (2017)

The synthesized Schiff base ligands H2L1, N,N'-bis(2-hydroxybenzylidene)1,2-diaminobenzene, and H2L2, N,N'-bis(2-hydroxybenzylidene)hydrazine, reacted with Alk2SnCl2 to give organotin(IV) complexes 1–10. The products were characterized by elemental analysis, FTIR, 1H and 13C NMR, and mass spectrometry. All organotin(IV) derivatives with [O,N,O] donor ligands retained their 5-coordinated geometry in solid state and solutions. Most of synthesized complexes exhibited significant antibacterial activity. Cytotoxicity was also tested by using the brine shrimp (Artemia salina) lethality bioassay.

Crystal structure, molecular docking, and treatment activity on myocarditis of a co-Schiff-base coordination polymer

Bai, Dong-Song,Bai, Li-Ying,Zhang, Qing-Shan,Zhao, Ming

, p. 782 - 788 (2020)

This work presents the synthesis and characterization of a dicyanamide-bridged coordination polymer {[Co2(L)2(dca)2](H2O)}n (named complex 1 hereafter) by using the N,O-donor Schiff base ligand 2-(((E

Thermodynamic properties of salophen schiff base + ionic liquid ([C nmIm][Br]) + dimethylformamide ternary mixtures at 298.15 K

Shekaari, Hemayat,Bezaatpour, Abolfazl,Elhami-Kalvanagh, Rasoul

, p. 345 - 351 (2012)

The densities and viscosities of ternary mixtures of N,N′- salicylidenephenylenediamine Schiff base (Salophen) + ionic liquid + N,N-dimethylformamide (DMF) have been determined at 298.15 K and at atmospheric pressure. The ionic liquids were: 1-propyl-3-me

Iron and cobalt salicylaldimine complexes as catalysts for epoxide and carbon dioxide coupling: effects of substituents on catalytic activity

Abu-Surrah, Adnan S.,Abdel-Halim, Hamzeh M.,Abu-Shehab, Hebah A. N.,Al-Ramahi, Esraa

, p. 117 - 122 (2017)

The synthesis and characterization of substituted ONNO-donor salen-type Schiff base complexes of general formula [MIII(L)Cl] (L?=?Schiff base ligand, M?=?Fe, Co) is reported. The complexes have been applied as catalysts for the coupling of carb

Spectroscopy studies on Schiff base N,N′-bis(salicylidene)-1,2-phenylenediamine by NMR, infrared, Raman and DFT calculations

De Toledo,Pizani,Da Silva,Teixeira,Freire

, p. 106 - 111 (2015)

N,N′-bis(salicylidene)-1,2-phenylenediamine, also known as Salophen, is a Schiff base which crystallizes in monoclinic structure and space group P21/c, with four molecules per unit cell. It has been intensely studied in last decades because of

2,2′-[Benzene-1,2-diylbis(iminomethanediyl)]diphenol derivative bearing two amine and hydroxyl groups as fluorescent receptor for Zinc(II) ion

Tayade, Kundan,Sahoo, Suban K.,Patil, Rahul,Singh, Narinder,Attarde, Sanjay,Kuwar, Anil

, p. 312 - 316 (2014)

A new non-natural receptor 2,2′-[benzene-1,2- diylbis(iminomethanediyl)]diphenol (4) was synthesized, and it is fluorogenic behaviour toward various metal ions were investigated. Receptor 4 exhibited pronounced fluorescence enhancement in the presence of

Cyanide Single-Molecule Magnets Exhibiting Solvent Dependent Reversible "on" and "off" Exchange Bias Behavior

Pinkowicz, Dawid,Southerland, Heather I.,Avenda?o, Carolina,Prosvirin, Andrey,Sanders, Codi,Wernsdorfer, Wolfgang,Pedersen, Kasper S.,Dreiser, Jan,Clérac, Rodolphe,Nehrkorn, Joscha,Simeoni, Giovanna G.,Schnegg, Alexander,Holldack, Karsten,Dunbar, Kim R.

, p. 14406 - 14422 (2015)

The syntheses, structures, and magnetic properties of four new complex salts, (PPN){[MnIII(salphen)(MeOH)]2[MIII(CN)6]}·7MeOH (Mn2M·7MeOH) (M = Fe, Ru, Os and Co; PPN+ = bis(triphenylphosph

Spectroscopic studies and keto-enol tautomeric effect of newer schiff bases of ortho-hydroxybenzaldehyde/ naphthaldehyde with 1,2-phenylenediamine and 4-aminophenyl ether

Shah, Ambreen,Shah, Asif A.

, p. 4215 - 4218 (2013)

Hydroxyl Schiff bases derived from 1,2-phenylenediamine and 4-aminophenyl ether with o-hydroxy benzaldehyde or o-hydroxyl naphthaldehyde were used to investigate enol-imine and keto-amine tautomeric analysis. UV-visible spectra of the compounds have been

Kinetics and mechanistic study of the reduction of Mn III by oxalate in Salophen scaffold: relevance to oxalate oxidase

Jena, Priyambada,Acharya, Achyuta N,Mundlapati, V Rao,Dash, Anadi C,Biswal, Himansu S

, (2018)

Abstract: The trans-Mn III(Salophen)(OH2)2+ and bioxalate (HOX -) in aqueous medium equilibrate rapidly to trans-Mn III(Salophen)(OH 2) (HOX) followed by the acid dissociation equilibrium to the (aqua) mono oxal

DNA interaction with Al-N,N′-bis(salicylidene)2,2′-phenylendiamine complex

Kashanian,Gholivand,Ahmadi,Taravati,Colagar, A. Hosseinzadeh

, p. 472 - 478 (2007)

The Al(III) complex, [Al(salophen)2H2O]NO3, was synthesized and characterized by spectroscopic (NMR and FT-IR) techniques. Then the binding of Schiff base complex of [Al(salophen)]+ type, where salophen denotes N,N′-bis(sa

Efficient red electroluminescent devices with sterically hindered phosphorescent platinum(II) Schiff base complexes and iridium complex codopant

Kwong, Chun-Lam,Kwok, Chi-Chung,Cheng, Gang,Che, Chi-Ming,Zhou, Liang,Zhang, Hongjie

, p. 2984 - 2994 (2014)

Sterically hindered platinum(II) Schiff base complexes were prepared. Complex 4, which displays red emission with a quantum yield of 0.29 in a thin film and a self-quenching rate constant of 1×10-7 dm3 mol-1 s-1

Salicylate-selective electrodes based on Al(III) and Sn(IV) salophens

Shahrokhian, Said,Amini, Mohammad K.,Kia, Reza,Tangestaninejad, Shahram

, p. 956 - 962 (2000)

New salicylate-selective electrodes based on aluminum(III) and tin(IV) salophens are described. The electrodes were prepared by incorporating the ionophores into plasticized poly(vinyl chloride) (PVC) membranes, which were directly coated on the surface of graphite electrodes. These novel electrodes display high selectivity for salicylate with respect to many common inorganic and organic anions. The influence of membrane composition and pH and the effect of lipophilic cationic and anionic additives on the response properties of the electrodes were investigated. The electrode based on- aluminum salophen, with 32% PVC, 65.8% plasticizer, and 2.2% ionophore, shows the best potentiometric response characteristics and displays a linear log [Sal-] vs EMF response over the concentration range 1 x 10-6-1 x 10-1 M in phosphate buffer solutions of pH 7.0, with a Nernstian slope of -59.2 mV/decade of salicylate concentration. Highest selectivity was observed for the membrane incorporating 38.8% PVC, 57.3% plasticizer, 2.6% Sn(salophen), and 1.3% sodium tetraphenylborate. The electrodes exhibit fast response times and micromolar detection limits (~1 x 10-6 M salicylate) and could be used over a wide pH range of 3-8. Applications of the electrodes for determination of salicylate in pharmaceutical preparations and biological samples are reported.

Gallium(III)-Salophen as a Dual Inhibitor of Pseudomonas aeruginosa Heme Sensing and Iron Acquisition

Ai, Yong,Centola, Garrick,Dent, Alecia T.,Deredge, Daniel J.,Hom, Kellie,Wilks, Angela,Xue, Fengtian

, p. 2073 - 2085 (2020)

Pseudomonas aeruginosa is an opportunistic bacterium that causes life-Threatening infections in immunocompromised patients. In infection, it uses heme as a primary iron source and senses the availability of exogenous heme through the heme assimilation sys

Coordination ability of free or silica immobilized Schiff bases towards Hg(II), Cd(II) and Pb(II) ions

Magro, Andrea,Crociani, Laura,Prinzivalli, Cristina,Vigato, Pietro Alessandro,Zanonato, Pier Luigi,Tamburini, Sergio

, p. 29 - 38 (2014)

A series of ligands, consisting of Schiff bases and their reduced amine derivatives, was prepared by [2+1] condensation of 3-methoxy (or 3-ethoxy)-2-hydroxybenzaldehyde or 2-hydroxybenzaldehyde with 3,4-diaminobenzoic acid or 1,2-diaminobenzene, and by su

Simple and rapid spectrophotometric determination of trace level chromium using bis (salicylaldehyde) orthophenylenediamine in nonionic micellar media

Soomro, Rubina,Ahmed, M. Jamaluddin,Memon, Najma

, p. 155 - 170 (2011)

Bis(salicylaldehyde)orthophenylenediamine (BSOPD) has been proposed as new analytical reagent for the direct spectrophotometric determination of chromium. It reacts with chromium(VI) in slightly acidic (0.1 - 0.3 M H2 SO4) micellar m

Chemoselective reduction of nitroaromatics using recyclable alumina-supported nickel nanoparticles in aqueous medium—exploration to one pot synthesis of benzimidazoles

Ghatak, Avishek,Bhar, Sanjay

supporting information, p. 368 - 379 (2022/02/05)

An economical and eco-compatible synthetic protocol for chemoselective and regioselective reduction of nitroaromatics in water has been achieved using easily accessible alumina-supported nickel nanoparticles as a stable recyclable heterogeneous catalyst. Various sensitive substituents like allyloxy, benzyloxy, t-butyldimethylsilyloxy, hydroxymethyl, alkoxycarbonyl, formyl, keto, carboxylic acid, chloro, bromo, azo and cyano were tolerated in the aforesaid protocol. This method has been extended for the construction of imidazole derivatives through one-pot reductive condensation of 2-nitroaniline with diversely substituted benzaldehydes. Some of the synthesized imidazoles have been used as antibacterial, antiplatelet and antithrombotic agents.

Synergistic effect of copper nanocrystals-nanoparticles incorporated in a porous organic polymer for the Ullmann C-O coupling r–eaction

Gorginpour, Forough,Zali-Boeini, Hassan

, (2021/02/22)

A quinoxaline-based porous organic polymer (Q-POP) as a mesoporous organic copolymer was developed as a new platform for the immobilization of CuNPs and copper nanocrystals. The prepared materials were characterized by FT-IR, XRD, N2 adsorption-desorption isotherms, ICP, TGA, SEM, HR-TEM, EDX, and single-crystal X-ray crystallography. The obtained catalyst presented extraordinary catalytic activity towards Ullmann C–O coupling reactions with high surface area, hierarchical porosity, and excellent thermal and chemical stability. Due to its high porosity, and synergistic effect of copper nanocrystals incorporated in the polymer composite, the as-synthesized catalyst was successfully utilized for the Ullmann C–O coupling reaction of phenols and different aryl halides to prepare various diaryl ether derivatives. All types of aryl halides (except aryl fluorides) were screened in the Ullmann C–O coupling reaction with phenols to produce diaryl ethers in good to excellent yields (70–97 %), and it was found that aryl iodides have the best results. Besides, due to the strong interactions between CuNPs, N, and O-atoms of quinoxaline moiety existing in the polymeric framework, the copper leaching from the support was not observed. Furthermore, the catalyst was recycled and reused for five consecutive runs without significant activity loss.

Efficient catalytic reduction of 4-nitrophenol using copper(Ii) complexes with n,o-chelating schiff base ligands

Abdullahi, Muhammad Sabiu,Endot, Nor Azam,Garba, Hassan Wafi,Jamil, Mohamad Shazwan Shah

, (2021/10/05)

The reduction of 4-nitrophenol to 4-aminophenol by sodium borohydride was used as a model to test the catalytic activity of copper(II) complexes containing N,O-chelating Schiff base ligands. In this study, a series of copper(II) complexes containing respective Schiff base ligands, N′-salicylidene-2-aminophenol (1), N′-salicylidene-2-aminothiazole (2), and N,N′-bis(salicylidene)-o-phenylenediamine (3), were synthesized and characterized by elemental analysis, Fourier transform infrared (FT-IR), and UV-Visible (UV-Vis) and electron paramagnetic resonance (EPR) spectroscopies. The results from the 4-nitrophenol reduction showed that 3 has the highest catalytic activities with 97.5% conversion, followed by 2 and 1 with 95.2% and 90.8% conversions, respectively. The optimiza-tion of the catalyst amount revealed that 1.0 mol% of the catalyst was the most optimized amount with the highest conversion compared to the other doses, 0.5 mol% and 1.5 mol%. Recyclability and reproducibility tests confirmed that all three complexes were active, efficient, and possess excellent reproducibility with consistent catalytic performances and could be used again without a major decrease in the catalytic activity.

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