Name: 1-(4-Nitrophenyl)ethanone. Recently I am researching about ATP CHANNEL OPENERS; FACILE SYNTHESIS; BIOLOGICAL-ACTIVITY; DERIVATIVES; SUBSTITUENTS; ARYLALKYNES; GENERATION; ALDEHYDES; BEARING; DESIGN, Saw an article supported by the . Published in AMER CHEMICAL SOC in WASHINGTON ,Authors: Tanaka, K; Kishimoto, M; Asada, Y; Tanaka, Y; Hoshino, Y; Honda, K. The CAS is 100-19-6. Through research, I have a further understanding and discovery of 1-(4-Nitrophenyl)ethanone
We report the one-pot synthesis of 2,2-disubstituted chromanes with electron-withdrawing substituents. This reaction provides a simple yet efficient route to a wide range of electron-deficient chromanes in high yield and excellent regioselectivity. The reaction of salicylaldehyde with 1,1-disubstituted ethylenes smoothly furnishes these electron-deficient chromanes, which can be further transformed into functionalized chromanes or chromene. For example, BW683C was effectively synthesized from 5-chlorosalicylaldehyde with 4-chlorostyrene in two steps in excellent yield. The present reaction thus provides versatile access to functionalized electron-deficient chromanes and chromenes and therefore constitutes a promising tool for the synthesis of biologically and photochemically active molecules.
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Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem