1620558-16-8

Basic information

• Product Name: ethyl 2-(4-(trifluoromethyl)phenyl)-1-(3-(2-oxopyrrolidin-1-yl)propyl)-1H-benzo[d]imidazole-5-carboxylate
• Synonyms: ethyl 2-(4-(trifluoromethyl)phenyl)-1-(3-(2-oxopyrrolidin-1-yl)propyl)-1H-benzo[d]imidazole-5-carboxylate
• CAS NO: 1620558-16-8
• Molecular Weight: 459.468
• Mol File: 1620558-16-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: ethyl 2-(4-(trifluoromethyl)phenyl)-1-(3-(2-oxopyrrolidin-1-yl)propyl)-1H-benzo[d]imidazole-5-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 2-(4-(trifluoromethyl)phenyl)-1-(3-(2-oxopyrrolidin-1-yl)propyl)-1H-benzo[d]imidazole-5-carboxylate(1620558-16-8)
• EPA Substance Registry System: ethyl 2-(4-(trifluoromethyl)phenyl)-1-(3-(2-oxopyrrolidin-1-yl)propyl)-1H-benzo[d]imidazole-5-carboxylate(1620558-16-8)

Safety Data

• Hazardous Substances Data: 1620558-16-8(Hazardous Substances Data)

Upstream product

• 455-19-6 4-Trifluoromethylbenzaldehyde 
• 152782-75-7 sodium hydroxy(4-(trifluoromethyl)phenyl)methanesulfonate 
• 1376395-94-6 C₁₆H₂₃N₃O₃ 
• 1620558-12-4 Ethyl 4-(3-(2-oxopyrrolidin-1-yl)propylamino)-3-nitrobenzoate 
• 453-71-4 3-nitro-4-fluorobenzoic acid 
• 367-80-6 ethyl 4-fluoro-3-nitrobenzoate 

Relevant articles and documents

Synthesis and evaluation of antimycobacterial activity of new benzimidazole aminoesters

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.