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ethyl 2-(4-nitrophenyl)-1-(3-(2-oxopyrrolidin-1-yl)propyl)-1H-benzo[d]imidazole-5-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1377136-59-8

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1377136-59-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1377136-59-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,7,1,3 and 6 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1377136-59:
(9*1)+(8*3)+(7*7)+(6*7)+(5*1)+(4*3)+(3*6)+(2*5)+(1*9)=178
178 % 10 = 8
So 1377136-59-8 is a valid CAS Registry Number.

1377136-59-8Downstream Products

1377136-59-8Relevant academic research and scientific papers

Synthesis and evaluation of antimycobacterial activity of new benzimidazole aminoesters

Yoon, Yeong Keng,Ali, Mohamed Ashraf,Wei, Ang Chee,Choon, Tan Soo,Ismail, Rusli

, p. 614 - 624 (2015/03/18)

Abstract A total of 51 novel benzimidazoles were synthesized by a 4-step reaction starting from basic compound 4-fluoro-3-nitrobenzoic acid under relatively mild reaction conditions. The structure of the novel benzimidazoles was confirmed by mass spectra as well as 1H NMR spectroscopic data. Out of the 51 novel synthesized compounds, 42 of them were screened for their antimycobacterial activity against Mycobacterium tuberculosis H37Rv strain using BacTiter-Glo Microbial Cell Viability (BTG) method. Results of activity screened using Alamar Blue method was also provided for comparison purposes. Two of the novel benzimidazoles synthesized showed moderately good activity with IC50 of less than 15 μM. Compound 5g, ethyl 2-(4-(trifluoromethyl)phenyl)-1-(2-morpholinoethyl)-1H-benzo[d]imidazole-5-carboxylate, was found to be the most active with IC50 of 11.52 μM.

Benzimidazoles as new scaffold of sirtuin inhibitors: Green synthesis, in vitro studies, molecular docking analysis and evaluation of their anti-cancer properties

Yoon, Yeong Keng,Ali, Mohamed Ashraf,Wei, Ang Chee,Shirazi, Amir Nasrolahi,Parang, Keykavous,Choon, Tan Soo

, p. 448 - 454 (2014/07/21)

Two series of novel benzimidazole derivatives were designed, synthesized and evaluated for their SIRT1 and SIRT2 inhibitory activity. Among the newly synthesized compounds, compound 4j displayed the best inhibitory activity for SIRT1 (IC50 = 54

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