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1,4-bis-(1,2,3-selenadiazole-4-yl)benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

132841-20-4

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132841-20-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 132841-20-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,8,4 and 1 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 132841-20:
(8*1)+(7*3)+(6*2)+(5*8)+(4*4)+(3*1)+(2*2)+(1*0)=104
104 % 10 = 4
So 132841-20-4 is a valid CAS Registry Number.

132841-20-4Downstream Products

132841-20-4Relevant academic research and scientific papers

Synthesis, characterization and antimicrobial activity of new 1,2,3-selenadiazoles

Al-Smadi, Mousa,Al-Momani, Fouad

experimental part, p. 2740 - 2749 (2009/04/11)

The commercially available aromatic polyketones 1a-d were utilized for the synthesis of the multi-arm 1,2,3-selenadiazole derivatives 3a-d. The preparation starts with the reaction between compounds 1a-d and p-toluenesulfonyl hydrazide to give the corresponding tosylhydrazones 2a-d. Subsequent reaction with selenium dioxide leads to regiospecific ring closure of the tosylhydrazones to give the target multi-arm 1,2,3-selenadiazole derivatives in high yield. A 1,2,3-selenadiazole derivative 3e containing an epoxide ring was also prepared. The structures of all the synthesized compounds were confirmed on the basis of spectral and analytical data. The compounds were screened in vitro for their antimicrobial activity against various pathogenic bacterial and Candida strains obtained from King Abdullah Hospital in Irbid -Jordan. Compounds 3a, 3c and 3e were found to be highly active against all the selected pathogens. Compound 3e showed an inhibition zone of 13 mm against the highly resistant P. aruginosa.

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