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4-[1-acetyl-2-oxoindolin-3-ylideneamino]benzenesulfanilamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

947253-66-9

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947253-66-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 947253-66-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,7,2,5 and 3 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 947253-66:
(8*9)+(7*4)+(6*7)+(5*2)+(4*5)+(3*3)+(2*6)+(1*6)=199
199 % 10 = 9
So 947253-66-9 is a valid CAS Registry Number.

947253-66-9Downstream Products

947253-66-9Relevant academic research and scientific papers

Metal based sulfanilamides: A note on their synthesis, spectral characterization, and antimicrobial activity

Rani,Sumrra,Chohan

, p. 1834 - 1842 (2017)

Objectives of the current study were synthesis, spectral characterization and biological screening of sulfanilamide derived Schiff bases and their metal based compounds. Sulfanilamide Schiff bases (L1–L3) were synthesized by condensation of 4-aminobenzenesulfanilamide with 1-(furan-2-yl)ethanone, 1-(thiophene-2-yl)-ethanone, and 1-acetylindoline-2,3-dione. The ligands were used for preparation of their Co(II), Ni(II), Cu(II), and Zn(II) complexes by using metals chlorides in metal: ligand (1: 2) molar ratio. All metal chelates had octahedral geometry with bidentate ligands. The ligands and their metal complexes were characterized by physical, spectral and analytical data, and screened for in-vitro antibacterial activity against six bacterial pathogens (Escherichia coli, Shigella flexneri, Pseudomonas aeruginosa, Salmonella typhi, Staphylococcus aureus, and Bacillus subtilis) and for in vitro antifungal activity against six fungal pathogens (Trichophyton longifusus, Candida albicans, Aspergillus flavus, Microsporum canis, Fusarium solani, and Candida glabrata). The results of antimicrobial studies revealed that the ligands activity was significantly increased upon chelation.

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