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Phenol, 2,2'-[1,2-ethanediylbis(iminomethylene)]bis[4-bromo- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

162586-73-4

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162586-73-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 162586-73-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,2,5,8 and 6 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 162586-73:
(8*1)+(7*6)+(6*2)+(5*5)+(4*8)+(3*6)+(2*7)+(1*3)=154
154 % 10 = 4
So 162586-73-4 is a valid CAS Registry Number.

162586-73-4Relevant academic research and scientific papers

Synthesis and antibacterial studies of some reduced schiff base derivatives

Patil, Udaysinha,Khan, Asif,Nagarsekar, Aarti,Mandewale, Mustapha,Yamgar, Ramesh

, p. 2796 - 2805 (2019/01/05)

A series of N,N-substituted ethylene-1,2-diamine derivatives have been prepared from reaction of 2-hydroxybenzaldehyde derivatives and 1,2-diamine derivatives in the presence of NaBH4 through Schiff base intermediate. The synthesized compounds were screened for their antibacterial activities. Compound SB01, SB02 and SB09 displayed significant activity at MIC ranges from 0.40-6.25 μg/mL.

Redox-active tetrahydrosalen (salan) complexes of titanium

Quiroz-Guzman, Mauricio,Oliver, Allen G.,Loza, Andrew J.,Brown, Seth N.

experimental part, p. 11458 - 11468 (2012/01/04)

A diarylamino-substituted N-methyl tetrahydrosalen (salan) ligand, An2NLH2, is prepared in four steps and overall 53% yield from 5-bromosalicylaldehyde, with the key step a palladium-catalysed Hartwig-Buchwald amination of the tert-b

Synthesis and antimicrobial activity of N,N′-bis(2-hydroxylbenzyl)-1, 2-ethanediamine derivatives

Musa, Musiliyu A.,Khan, M. Omar F.,Aspedon, Arden,Cooperwood, John S.

experimental part, p. 165 - 170 (2011/02/23)

A series of N,N′-Bis(2-hydroxylbenzyl)-1,2-ethanediamine derivatives and its schiff bases were synthesized, characterized and screened for in vitro antimicrobial activity against Staphylococcus aureus, Pseudomonas aeruginosa and Salmonella enterica. Resul

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