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N-2,5-dichlorophenyl-N'-nicotinoyl thiourea is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1417441-29-2

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1417441-29-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1417441-29-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,7,4,4 and 1 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1417441-29:
(9*1)+(8*4)+(7*1)+(6*7)+(5*4)+(4*4)+(3*1)+(2*2)+(1*9)=142
142 % 10 = 2
So 1417441-29-2 is a valid CAS Registry Number.

1417441-29-2Downstream Products

1417441-29-2Relevant academic research and scientific papers

Synthesis and biological evaluation of 3-amino-1,2,4-triazole derivatives as potential anticancer compounds

Benhida, Rachid,Demange, Luc,Dufies, Maeva,Grytsai, Oleksandr,Hagege, Anais,Martial, Sonia,Pagès, Gilles,Penco-Campillo, Manon,Ronco, Cyril,Valiashko, Oksana

, (2020)

Two series of compounds carrying 3-amino-1,2,4-triazole scaffold were synthesized and evaluated for their anticancer activity against a panel of cancer cell lines using XTT assay. The 1,2,4-triazole synthesis was revisited for the first series of pyridyl derivatives. The biological results revealed the efficiency of the 3-amino-1,2,4-triazole core that could not be replaced and a clear beneficial effect of a 3-bromophenylamino moiety in position 3 of the triazole for both series (compounds 2.6 and 4.6) on several cell lines tested. Moreover, our results point out an antiangiogenic activity of these compounds. Overall, the 5-aryl-3-phenylamino-1,2,4-triazole structure has promising dual anticancer activity.

Microwave assisted synthesis and biological activity of n-aryl-n'-nicotinoyl thiourea

Tong, Jian-Ying,Sun, Na-Bo,Wu, Hong-Ke

, p. 5420 - 5422 (2013/07/26)

A series of N-aryl-N'-nicotinoyl thiourea derivatives were synthesized using microwave irradiation. The synthesized compounds were characterized by 1H NMR, IR, MS and elemental analysis. Fungicidal activity of the compounds were evaluated through G. zeae

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