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2-(5-nitroisoquinolin-6-yl)-4,5-dimethoxybenzoic acid methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1201566-89-3

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1201566-89-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1201566-89-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,1,5,6 and 6 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1201566-89:
(9*1)+(8*2)+(7*0)+(6*1)+(5*5)+(4*6)+(3*6)+(2*8)+(1*9)=123
123 % 10 = 3
So 1201566-89-3 is a valid CAS Registry Number.

1201566-89-3Downstream Products

1201566-89-3Relevant academic research and scientific papers

Synthesis and biological evaluation of N-substituted benzo[c] phenanthrolines and benzo[c]phenanthrolinones as antiproliferative agents

Genès, Constance,Lenglet, Ga?lle,Depauw, Sabine,Nhili, Raja,Prado, Soizic,David-Cordonnier, Marie-Hélène,Michel, Sylvie,Tillequin, Fran?ois,Porée, Fran?ois-Hugues

, p. 2117 - 2131 (2011/06/21)

Benzo[c]phenanthrolines and benzo[c]phenanthrolinones substituted by dialkylaminoalkyl side chains at position N5 and C6, respectively, were synthesised and their biological activity evaluated. They displayed interessant cytotoxicity associated with some DNA interactions. However, the low topoisomerase 1 affinity suggests that other cellular targets are responsible for the antiproliferative activity.

Synthesis of N-substituted benzo[c][1,7]- and benzo[c][1,8] phenanthrolin-(5H)-6-ones through a Pd-mediated Suzuki-Miyaura heteroaryl-aryl coupling reaction

Genès, Constance,Michel, Sylvie,Tillequin, Fran?ois,Porée, Fran?ois-Hugues

experimental part, p. 10009 - 10015 (2010/02/27)

In the course of the search for non-camptothecin topoisomerase I inhibitors we have undertaken the synthesis of N-substituted benzo[c][1,7]- and benzo[c][1,8]phenanthrolinone derivatives. An intermolecular Suzuki-Miyaura heteroaryl-aryl coupling reaction was planned as the key step. Then a nitro reduction followed by a concomitant lactamization achieved the construction of the tetracycle structures. This methodology permitted a rapid and efficient elaboration of biologically potent compounds.

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