78036-47-2

Usage

Uses

Used in Materials Science:
(N1Z,N2Z)-N1,N2-Bis(4-Bromobenzylidene)Ethane-1,2-Diamine is used as a building block for the synthesis of coordination polymers and metal-organic frameworks for their unique properties and potential applications in various fields, such as gas storage, catalysis, and drug delivery.
Used in Corrosion Inhibition:
(N1Z,N2Z)-N1,N2-Bis(4-Bromobenzylidene)Ethane-1,2-Diamine is used as a corrosion inhibitor for metals to protect them from degradation and extend their service life in various industrial applications.
Used in Antifungal Applications:
(N1Z,N2Z)-N1,N2-Bis(4-Bromobenzylidene)Ethane-1,2-Diamine is used as a potential antifungal agent for its ability to inhibit the growth of fungi, which can be beneficial in the medical and agricultural industries to control fungal infections and contamination.
Used in Pharmaceutical Industry:
(N1Z,N2Z)-N1,N2-Bis(4-Bromobenzylidene)Ethane-1,2-Diamine is used as a starting material or intermediate in the synthesis of various pharmaceutical compounds due to its unique structural features and potential for medicinal applications.
Used in Chemical Research:
(N1Z,N2Z)-N1,N2-Bis(4-Bromobenzylidene)Ethane-1,2-Diamine is used as a research compound for studying its properties and potential applications in various fields, including materials science, medicinal chemistry, and corrosion science.

Upstream product

• 1122-91-4 4-bromo-benzaldehyde 
• 107-15-3 ethylenediamine 
• 138023-09-3 N-(4-bromobenzylidene)pyridin-2-amine 

Downstream Products

• 2551-54-4 N¹,N²-bis(4-bromobenzyl)ethane-1,2-diamine 
• 2551-58-8 1,3-bis-(4-bromo-benzyl)-2-isopropyl-imidazolidine 
• 2551-55-5 1,3-bis-(4-bromo-benzyl)-2-methyl-imidazolidine 
• 2691-43-2 2-ethyl-1,3-bis-(4-bromo-benzyl)-imidazolidine 
• 2551-57-7 1,3-bis-(4-bromo-benzyl)-2-propyl-imidazolidine 
• 2551-56-6 1,3-bis-(4-bromo-benzyl)-2-trichloromethyl-imidazolidine 
• 2571-30-4 1,3-bis-(4-bromo-benzyl)-2-phenyl-imidazolidine 
• 2513-53-3 1,3-bis-(4-bromo-benzyl)-2-(4-bromo-phenyl)-imidazolidine 
• 2513-58-8 4-[1,3-bis-(4-bromo-benzyl)-imidazolidin-2-yl]-phenol 
• 2513-55-5 1,3-bis-(4-bromo-benzyl)-2-(3-chloro-phenyl)-imidazolidine 
• 2513-56-6 1,3-bis-(4-bromo-benzyl)-2-(3-iodo-phenyl)-imidazolidine 
• 2513-54-4 1,3-bis-(4-bromo-benzyl)-2-(2-chloro-phenyl)-imidazolidine 
• 2513-57-7 2-[1,3-bis-(4-bromo-benzyl)-imidazolidin-2-yl]-phenol 
• 2513-60-2 1,3-bis-(4-bromo-benzyl)-2-(3-nitro-phenyl)-imidazolidine 

Relevant academic research and scientific papers

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

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.

Achiral bis-imine in combination with CoCI2: A remarkable effect on enantioselectivity of lipasemediated acetylation of racemic secondary alcohol

A bis-imine (prepared via a new FeCl3-based method) in combination with CoCl2 facilitated lipase-mediated acetylation of the (R)-isomer of a racemic benzylic secondary alcohol with 91% ees. The methodology was used for the preparation of the known drug rivastigmine.

Studies on the Oxidation of the Azomethine Compounds with 3-Chloroperbenzoic Acid

Oxidation of the azomethine compounds such as Schiff bases and azines having several nucleophilic centers with 3-chloroperbenzoic acid (MCPBA) being an electrophilic oxidant was investigated.From azines 4, bisaldimines 5, 6, and pyridine derived monoaldimines 7, 8, having various substituents on the imine carbon and nitrogen atoms, the products such as nitrones 9, 15, bisoxaziridines 11, 12; acyldiimine 10 and amide 14 were obtained in high yields.The influence of the structure of substrate on the reaction result is discussed.Key words: aldimines, azines, nitrones, oxaziridines