Our Top Choice Compound:1-(4-Nitrophenyl)ethanone

About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Monsen, PJ; Luzzio, FA or concate me.. Formula: C8H7NO3

Authors Monsen, PJ; Luzzio, FA in PERGAMON-ELSEVIER SCIENCE LTD published article about PORPHYROMONAS-GINGIVALIS ADHERENCE; 1,2,3-TRIAZOLE-BASED INHIBITORS; ORAL STREPTOCOCCI; PROSTAGLANDINS in [Monsen, Paige J.; Luzzio, Frederick A.] Univ Louisville, Dept Chem, 2320 South Brook St, Louisville, KY 40292 USA in 2020, Cited 25. Formula: C8H7NO3. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6

An array of arylnitro compounds with various functionality were treated with freshly-prepared aluminum amalgam in THE/water solution and resulted in the corresponding arylamines. The Al(Hg)-mediated reductions are relatively rapid with consumption of the amalgam and disappearance of starting material occurring over 20-30 min. The workup of the reductions involves only removal of the insoluble by-products by filtration followed by concentration. Only in some cases is chromatography required to secure the pure product. The desired arylamines are furnished in quantities of 25-100 mg, which in some cases, could be taken on to the next reaction without further purification. Reductions of 4-nitrobenzyl derivatives of carbohydrates or nucleosides were selective in affording the corresponding 4-aminobenzyl products. To show applicability in click chemistry, selected aminobenzyl products are directly azidated to yield products that were then used in click reactions to afford the corresponding 1,2,3-triazoles. (C) 2020 Elsevier Ltd. All rights reserved.

About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Monsen, PJ; Luzzio, FA or concate me.. Formula: C8H7NO3

Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem