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1-[2-(3-nitrophenyl)-2-oxoethyl]-2-[(morpholine-4-yl)thioxomethyl]benzimidazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1449313-08-9

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1449313-08-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1449313-08-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,9,3,1 and 3 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1449313-08:
(9*1)+(8*4)+(7*4)+(6*9)+(5*3)+(4*1)+(3*3)+(2*0)+(1*8)=159
159 % 10 = 9
So 1449313-08-9 is a valid CAS Registry Number.

1449313-08-9Downstream Products

1449313-08-9Relevant academic research and scientific papers

Synthesis and biological evaluation of some 1,2-disubstituted benzimidazole derivatives as new potential anticancer agents

Yurttas, Leyla,Demirayak, Seref,Ciftci, Guelsen A.,Yildirim, Safak Ulusoylar,Kaplancikli, Zafer A.

, p. 403 - 414 (2013/07/25)

The synthesis of some new 1-(2-aryl-2-oxoethyl)-2-[(morpholine-4-yl) thioxomethyl]benzimidazole derivatives and investigation of their anticancer activities were the aims of this work. 2-(Chloromethyl)benzimidazole compound was reacted with sulfur and morpholine via Willgerodt-Kindler reaction to give 2-[(morpholine-4-yl)thioxomethyl]benzimidazole. Then, the obtained compound was reacted with appropriate α-bromoacetophenone derivatives in the presence of potassium carbonate to give the final products. Structure elucidation of the final compounds was achieved by FT-IR, 1H NMR spectroscopy and MS spectrometry. The anticancer activities of the final compounds were evaluated by MTT assay, BrdU method, and flow cytometric analysis on C6, MCF-7, and A549 tumor cells. Most of the synthesized compounds exhibited considerable selectivity against the MCF-7 and C6 cell lines. New 1-(2-aryl-2-oxoethyl)-2- [(morpholine-4-yl)thioxomethyl]benzimidazole derivatives were synthesized and investigated for their anticancer activities against C6, MCF-7, and A549 tumor cells. Most of the synthesized compounds exhibited considerable selectivity against the MCF-7 and C6 cell lines. Copyright

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