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3-Phenylimidazo<1,2-f>phenanthridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

132141-40-3

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132141-40-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 132141-40-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,1,4 and 1 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 132141-40:
(8*1)+(7*3)+(6*2)+(5*1)+(4*4)+(3*1)+(2*4)+(1*0)=73
73 % 10 = 3
So 132141-40-3 is a valid CAS Registry Number.

132141-40-3Downstream Products

132141-40-3Relevant academic research and scientific papers

Synthesis of 6-aminophenanthridines via palladium-catalyzed insertion of isocyanides into N-sulfonyl-2-aminobiaryls

Jiang, Huanfeng,Gao, Hanling,Liu, Bifu,Wu, Wanqing

, p. 17222 - 17225 (2014)

A robust route to a diverse set of 6-aminophenanthridines via palladium-catalyzed C-H activation of N-sulfonyl-2-aminobiaryl and isocyanide insertion is reported. This transformation could also provide an important approach for building core frameworks of conjugated organic polymer materials.

Synthesis of imidazo[1,2-f]phenanthridine derivatives under a metal- and base-free condition and their anticancer activity

Narva, Suresh,Zhang, Mi,Li, Ce,Chen, An,Tanaka, Yoshimasa,Zhang, Wen

, (2021)

A series of imidazo[1,2-f]phenanthridine derivatives were synthesized from phenanthridin-6-amine and aldehydes through sulfur endorsed oxidative cyclization reaction under a metal- and base-free condition with atom economy strategy and evaluated their anticancer activity. Among all the synthesized derivatives, the compound 3d and 3f exhibited IC50 values of 2.18 ± 0.08 and 2.24 μM ± 0.71 μM, respectively. Compound 3d had the strongest inhibitory activity against HT-29 cells with an IC50 value being 1.25 μM ± 0.22 μM, which was even stronger than that of paclitaxel.

Electrochemical Cyclization of 1-Phenyl-2(-1'-chlorophenyl)-substituted Five-membered Nitrogen Heterocycles. Application to the Synthesis of Phenanthridines

Grimshaw, James,Hewitt, S. Armstrong

, p. 2995 - 2998 (2007/10/02)

Pyrrolophenanthridine (compound 4), 3-phenylimidazophenanthridine 8, tetrazolophenanthridine 11 and benzotetrazolophenanthridine 12 have been prepared using an electrochemical cyclizatin procedure.Treatment of the imidazophenanthridine with singlet oxygen yields a phenanthridone by degradation of the heterocyclic system.Lithium aluminium hydride reduction of the tetrazolophenanthridines yields the phenanthridine.

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