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1-Ethoxy-3-(2-nitro-ethyl)-benzene is an organic compound with the molecular formula C10H13NO3. It is a derivative of benzene, featuring an ethoxy group (C2H5O) attached to the first carbon atom and a 2-nitro-ethyl group (C2H4NO2) attached to the third carbon atom. 1-ethoxy-3-(2-nitro-ethyl)-benzene is characterized by its aromatic structure, with the nitro group providing a strong oxidizing property and the ethoxy group contributing to its solubility in organic solvents. It is used in various chemical reactions and synthesis processes, particularly in the preparation of pharmaceuticals and other organic compounds. Due to its reactive groups, it is essential to handle 1-ethoxy-3-(2-nitro-ethyl)-benzene with care, following proper safety protocols to minimize potential hazards.

3159-51-1

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3159-51-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3159-51-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,5 and 9 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3159-51:
(6*3)+(5*1)+(4*5)+(3*9)+(2*5)+(1*1)=81
81 % 10 = 1
So 3159-51-1 is a valid CAS Registry Number.

3159-51-1Relevant academic research and scientific papers

Substitution of terminal amide with 1H-1,2,3-triazole: Identification of unexpected class of potent antibacterial agents

Bi, Fangchao,Ji, Shengli,Venter, Henrietta,Liu, Jingru,Semple, Susan J.,Ma, Shutao

supporting information, p. 884 - 891 (2018/02/15)

3-Methoxybenzamide (3-MBA) derivatives have been identified as novel class of potent antibacterial agents targeting the bacterial cell division protein FtsZ. As one of isosteres for the amide group, 1,2,3-triazole can mimic the topological and electronic features of the amide, which has gained increasing attention in drug discovery. Based on these considerations, we prepared a series of 1H-1,2,3-triazole-containing 3-MBA analogues via isosteric replacement of the terminal amide with triazole, which had increased antibacterial activity. This study demonstrated the possibility of developing the 1H-1,2,3-triazole group as a terminal amide-mimetic element which was capable of both keeping and modulating amide-related bioactivity. Surprisingly, a different action mode of these new 1H-1,2,3-triazole-containing analogues was observed, which could open new opportunities for the development of antibacterial agents.

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