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N-(4-methylbenzylidene)-N-{2-[(4-methylbenzylidene)amino]ethyl}amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 552859-12-8 Structure
  • Basic information

    1. Product Name: N-(4-methylbenzylidene)-N-{2-[(4-methylbenzylidene)amino]ethyl}amine
    2. Synonyms: N-(4-methylbenzylidene)-N-{2-[(4-methylbenzylidene)amino]ethyl}amine
    3. CAS NO:552859-12-8
    4. Molecular Formula: C18H20N2
    5. Molecular Weight: 264.3648
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 552859-12-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: N-(4-methylbenzylidene)-N-{2-[(4-methylbenzylidene)amino]ethyl}amine(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(4-methylbenzylidene)-N-{2-[(4-methylbenzylidene)amino]ethyl}amine(552859-12-8)
    11. EPA Substance Registry System: N-(4-methylbenzylidene)-N-{2-[(4-methylbenzylidene)amino]ethyl}amine(552859-12-8)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 552859-12-8(Hazardous Substances Data)

552859-12-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 552859-12-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,5,2,8,5 and 9 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 552859-12:
(8*5)+(7*5)+(6*2)+(5*8)+(4*5)+(3*9)+(2*1)+(1*2)=178
178 % 10 = 8
So 552859-12-8 is a valid CAS Registry Number.

552859-12-8Relevant articles and documents

Facile access to polymer supported zinc–salen complex: highly efficient heterogeneous catalyst for synthesizing hydantoins, thiohydantoins and Schiff bases in aqueous medium

Balinge, Kamlesh Rudreshwar,Khiratkar, Avinash Ganesh,Muskawar, Prashant Narayan,Thenmozhi,Bhagat, Pundlik Rambhau

, p. 2075 - 2097 (2017/12/26)

The synthesis of polymer supported zinc–salen complex (PS-Zn–salen) is described. The mononuclear zinc(II)–salen complex was characterized by Fourier-transform NMR spectroscopy, energy-dispersive X-ray spectroscopy, Fourier transform infrared spectrophotometry (FT-IR), thermogravimetric analysis, scanning electron microscopy, surface area and pore size distribution by Brunauer–Emmett–Teller. The synthesized PS-Zn–salen complex used as a recyclable heterogeneous catalyst for the efficient synthesis of hydantoins, thiohydantoins and Schiff bases in an aqueous medium. The isolated yields of hydantoins, thiohydantoins and Schiff bases achieved up to 89, 95 and 94%, respectively. In spite of conventional heterogeneous catalysts, current PS-Zn–salen complex shows thermal stability up to 280?°C. Moreover, the catalyst could be recovered easily by simple filtration and reused for next run with slightly declining its activity up to six successive runs. The FT-IR spectrum of recycle catalyst after 6th run confirmed that the catalyst was stable during the course of a reaction. The leaching of metal from the PS-Zn–salen is negligible, which was confirmed by AAS and hot filtration test.

One-pot synthesis of imidazolinium salts via the ring opening of tetrahydrofuran

Huang, Yong-Qing,Zhao, Yue,Wang, Peng,Okamura, Taka-Aki,Laforteza, Brian N.,Lu, Yi,Sun, Wei-Yin,Yu, Jin-Quan

supporting information, p. 12430 - 12433 (2017/10/06)

A new one-pot synthesis of C2-hydroxypropyl-substituted imidazolinium salts via the ring opening of tetrahydrofuran (THF) with N,N′-disubstituted diamines has been developed. Preliminary studies of the reaction mechanism suggest the CO2-promoted oxidative ring opening of THF followed by Hg(ii)-mediated oxidation of an imidazolidine intermediate. These novel C2-substituted imidazolinium salts have shown to be active catalysts for the aza-Diels-Alder reactions.

Synthesis, ir and nmr spectral correlations in some symmetrical diimines

Thirunarayanan

, p. 73 - 79 (2014/03/21)

A series of diimines have been synthesized by coupling of diamine with substituted benzaldehydes. The purities of these diimines were checked by their analytical and spectroscopic data. The spectral frequencies vCN (cm-1), NMR chemical shifts (v, ppm) of C-H and C=N of these diimines have been correlated with Hammett substituent constants, F and R parameters using single and multi-linear regression analysis. From the results of statistical analysis, the effect of substituents on the above spectral data has been studied.

Synthesis of new antifungal 1,2,4-bis-oxadiazolines using cycloaddition reaction of nitrile oxide with bis-Schiff base

Toumi, Ahmed,Daami-Remadi, Mejda,Jannet, Hichem Ben

, p. 922 - 928 (2013/08/15)

A series of arylaldehydes and acetophenone when treated with 1,2-ethanediamine afford the bis-Schiff bases N,N'- bis(arylidene)-ethane-l,2- diamines 1-8, N,N'-bis(arylmethylene)-ethane-l,2-diamines 9-10 and the N,N'-bis(l- phenylethylidene)-ethane-l,2-dia

Synthesis and biological evaluation of novel substituted-imidazolidine derivatives

Husain, Asif,Bhutani, Rubina,Kumar, Deepak,Shin, Dong-Soo

, p. 227 - 233 (2013/07/26)

A series of newer substituted-imidazolidine derivatives 3a-k were synthesized and assayed in vivo to investigate their anti-inflammatory, analgesic and antiulcer activity. The results of biological evaluation revealed that the three compounds, 4-[1,3-bis(4-hydroxy-3-methoxybenzyl)-2- imidazolidinyl]phenyldiethylamine (3g), 4-[1,3-bis(3-Ethoxy-4-hydroxybenzyl)-2- imidazolidinyl] phenyldiethylamine (3h) and 4-(1,3-bis(benzo[d][1,3]dioxol-5- ylmethyl)-4-methylimidazolidin-2-yl)-N,N-diethylbenzenamine (3j) were good in their anti-inflammatory and analgesic actions. Additionally these derivatives showed superior GI safety profile as compared to that of the standard drug in terms of low severity index. The results are statistically treated for its significance.

Preparation of a series of Ru(ii) complexes with N-heterocyclic carbene ligands for the catalytic transfer hydrogenation of aromatic ketones

Guerbuez, Nevin,Oezcan, Emine Oezge,Oezdemir, Ismail,Cetinkaya, Bekir,Sahin, Onur,Bueyuekguengoer, Orhan

experimental part, p. 2330 - 2339 (2012/03/22)

The reaction of [RuCl2(p-cymene]2 with Ag-N-heterocyclic carbene (NHC) complexes yields a series of [(p-cymene)Ru(NHC)] complexes (2a-f). All synthesised compounds were characterized by elemental analysis, NMR spectroscopy and the mo

Zn2+-K10-clay (clayzic) as an efficient water-tolerant, solid acid catalyst for the synthesis of benzimidazoles and quinoxalines at room temperature

Dhakshinamoorthy, Amarajothi,Kanagaraj, Kuppusamy,Pitchumani, Kasi

supporting information; scheme or table, p. 69 - 73 (2011/02/25)

A very simple, green and efficient protocol is developed in which zinc chloride-exchanged K10-montmorillonite (clayzic) is employed as a Lewis acid catalyst in aqueous media at room temperature for the synthesis of various benzimidazoles and quinoxalines from carbonyl compounds and o-phenylenediamine. Among the various catalysts (including claycop and Zn2+-Y) studied, clayzic produces benzimidazoles and quinoxalines in higher yield, and with a flexible diamine such as ethylenediamine only the bis-Schiff base is formed. Other salient features of this protocol include milder conditions, atom-economy, absence of coupling agents, and no wastes.

Synthesis, antimicrobial activity and structure-activity relationship study of N,N-dibenzyl-cyclohexane-1,2-diamine derivatives

Sharma, Mukul,Joshi, Penny,Kumar, Nitin,Joshi, Seema,Rohilla, Rajesh K.,Roy, Nilanjan,Rawat, Diwan S.

experimental part, p. 480 - 487 (2011/03/19)

We report herein synthesis and antimicrobial activity of a series of N,N-dibenzyl-cyclohexane-1,2-diamine derivatives. In order to study the structure-activity relationship of substituted dibenzyl-cyclohexane-1,2-diamine derivatives, 44 structurally diverse compounds were synthesized and tested against Gram-positive and Gram-negative bacterial strains. Among them, compounds 17-20, 26, 37, 38 were found to be more active than tetracycline with MIC value ranging 0.0005-0.032 μg/mL and no hemolysis upto 1024 μg/mL in mammalian erythrocytes was observed. Some of the compounds have also shown very promising antifungal activity against Candida albicans, Candida glabrata and Geotrichum candidium.

Synthesis, spectroscopic studies and crystal structures of ReI(CO)3(NN)Cl complexes with N,Nae-bis(substituted benzylidene)ethane-1,2-diamine Schiff base ligands

Mirkhani, Valiollah,Kia, Reza,Milic, Dalibor,Vartooni, Akbar Rostami,Matkovic-Calogovic, Dubravka

experimental part, p. 81 - 87 (2011/12/14)

Four new Re(I) tricarbonyl-diimine complexes were prepared by reaction of Re(CO)5Cl with N,Nae-bis(substituted benzylidene)ethane-1,2-diamine Schiff base ligands. These compounds were characterized by physico-chemical methods, and their crystal

Synthesis of [N, N'-Bis(5-benzoyl-4-phenylthiazol-2-yl)-N, N-bisbenzyl]ethane-1, 2-diamines

Asha,Manju,Pradeep,George,Rajasekharan

scheme or table, p. 1726 - 1730 (2009/05/30)

Synthesis of [N,N'-bis(N-benzoylthiocarbamoyl)-N,N'-bis(benzyl)]ethane-1,2- diamines 4a-h, their cyclization to [N,N'-bis(5-benzoyl-4-phenylthiazol-2-yl)-N, N'-bisbenzyl]ethane-1,2-diamines 5a-h by reaction with phenacyl bromide and the results of antibacterial activity assay of 4a-h and 5a-h are reported.

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