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(p-methoxy-benzyliden)-selenosemicarbazide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

17222-74-1

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17222-74-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17222-74-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,2,2 and 2 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 17222-74:
(7*1)+(6*7)+(5*2)+(4*2)+(3*2)+(2*7)+(1*4)=91
91 % 10 = 1
So 17222-74-1 is a valid CAS Registry Number.

17222-74-1Relevant academic research and scientific papers

New approach towards the synthesis of selenosemicarbazones, useful compounds for Chagas' disease

Pizzo, Chiara,Faral-Tello, Paula,Yaluff, Gloria,Serna, Elva,Torres, Susana,Vera, Ninfa,Saiz, Cecilia,Robello, Carlos,Mahler, Graciela

, p. 107 - 113 (2016/01/15)

Herein, we describe a new approach towards the synthesis of selenosemicarbazones. The reaction involves an O-Se exchange of semicarbazones using Ishihara reagent. Eleven selenosemicarbazones were prepared using this methodology, with low to moderate yields. Among the prepared compounds the m-bromo phenyl methyl derivative 1b was selected to be evaluated in vivo, in a murine model of acute Chagas' disease. Compound 1b 10 mg/kg bw/day reduced 50% of parasitaemia profile compared with the control group, but was less effective than Benznidazole (50 mg/kg bw/day reduced 90%) and toxic. These studies are important to guide future Chagas drug design.

Heterocycles 23: Synthesis, characterization and anticancer activity of new hydrazinoselenazole derivatives

Zaharia, Valentin,Ignat, Adriana,Ngameni, Bathelemy,Kuete, Victor,Moungang, Marlyse L.,Fokunang, Charles N.,Vasilescu, Mihai,Palibroda, Nicolae,Cristea, Castelia,Silaghi-Dumitrescu, Luminita,Ngadjui, Bonaventure T.

, p. 5670 - 5679 (2013/11/06)

A series of novel functionalized 1,3-selenazole was synthesized by Hantzsch-type condensation reaction and evaluated for their in vitro cytotoxic activity against two human cancer cell lines. The structures of the synthesized selenosemicarbazones and func

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