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2-(2-methyl-4-nitro-1H-imidazol-1-yl)-N-(4-nitrophenyl)acetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

415938-78-2

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415938-78-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 415938-78-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,1,5,9,3 and 8 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 415938-78:
(8*4)+(7*1)+(6*5)+(5*9)+(4*3)+(3*8)+(2*7)+(1*8)=172
172 % 10 = 2
So 415938-78-2 is a valid CAS Registry Number.

415938-78-2Downstream Products

415938-78-2Relevant academic research and scientific papers

Synthesis and in vitro trichomonicidal, giardicidal and amebicidal activity of N-acetamide(sulfonamide)-2-methyl-4-nitro-1H-imidazoles

Hernandez-Nunez, Emanuel,Tlahuext, Hugo,Moo-Puc, Rosa,Torres-Gomez, Hector,Reyes-Martinez, Reyna,Cedillo-Rivera, Roberto,Nava-Zuazo, Carlos,Navarrete-Vazquez, Gabriel

, p. 2975 - 2984 (2009)

Two new series of imidazole derivatives (acetamides: 1-8 and sulfonamides: 9-15) were synthesized using a short synthetic route. Compound 1 as well as the intermediate 16g were characterized by X-ray crystallography. Imidazole derivatives 1-15 were tested in vitro against three unicellular parasites (Giardia intestinalis, Trichomonas vaginalis and Entamoeba histolytica) in comparison with benznidazole (Bzn) and metronidazole. Compound 1 [N-benzyl-2-(2-methyl-4-nitro-1H-imidazol-1-yl)acetamide] was 2 times more active than Bzn against T. vaginalis and G. intestinalis and it was as active as Bzn against E. histolytica. Sulfonamides showed selective toxicity against E. histolytica over the other parasites. Toxicity assay showed that all compounds are non-cytotoxic against MDCK cell line. The results revealed that compounds 1-15 have antiparasitic bioactivity in the micromolar range against the parasites tested, and could be considered as benznidazole bioisosteres.

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