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N,N'-[4,4'-sulfonylbis(4,1-phenylene)]bis(2-cyano-2-(1,3-dithiolan-2-ylidene)acetamide) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1415906-29-4

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1415906-29-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1415906-29-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,5,9,0 and 6 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1415906-29:
(9*1)+(8*4)+(7*1)+(6*5)+(5*9)+(4*0)+(3*6)+(2*2)+(1*9)=154
154 % 10 = 4
So 1415906-29-4 is a valid CAS Registry Number.

1415906-29-4Downstream Products

1415906-29-4Relevant academic research and scientific papers

Dapson in heterocyclic chemistry, part V: Synthesis, molecular docking and anticancer activity of some novel sulfonylbiscompounds carrying biologically active dihydropyridine, dihydroisoquinoline, 1,3-dithiolan, 1,3-dithian, acrylamide, pyrazole, pyrazolopyrimidineand benzochromenemoieties

Ghorab, Mostafa Mohammed,Al-Said, Mansour Sulaiman,Nissan, Yassin Mohammed

, p. 1019 - 1028 (2012)

N,N′-(4,4′-Sulfonylbis(4,1-phenylene))bis(2-cyanoacetamid) 2 was utilized as a key intermediate for the synthesis of novel dihydropyridines 3, 4, 8, dihydroisoquinolines 5-7, dithiolan 10, dithian 11, acrylamide 12, benzochromenes 17 and 18 and chromenopyridones 19 and 20. Compound 2 was the starting material in the synthesis of the acrylamide derivative 14, the pyrazole derivative 15 and the pyrazolopyrimidine derivative 16. All the synthesized compounds were evaluated for their in vitro anticancer activity against human breast cancer cell line (MCF7). Compound 19 showed the best cytotoxic activity with IC50 value 19.36 μM. In addition, molecular docking study of the synthesized compounds on the active sites of farnesyltransferase and arginine methyltransferase was performed in order to give a suggestion about the mechanism of action of their cytotoxic activity.

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