67323-06-2

Usage

Uses

Used in Pharmaceutical Synthesis:
4'-Methoxy-2'-nitroacetophenone is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique chemical structure allows for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Production:
4'-METHOXY-2'-NITROACETOPHENONE also plays a crucial role in the production of agrochemicals, contributing to the development of effective pesticides and other agricultural chemicals that enhance crop protection and yield.
Used in Dye and Pigment Manufacturing:
4'-Methoxy-2'-nitroacetophenone is utilized as an intermediate in the manufacturing of dyes and pigments, providing a range of color options for various industries, including textiles, plastics, and printing inks.
Used in Organic Synthesis Research:
In the field of research, 4'-Methoxy-2'-nitroacetophenone is employed as a building block for the synthesis of complex organic compounds. Its electron-withdrawing properties make it a valuable tool for exploring new chemical reactions and developing innovative synthetic pathways.
Used in Industrial Applications:
4'-METHOXY-2'-NITROACETOPHENONE's versatility and reactivity make it suitable for various industrial applications, where it is used to produce a wide range of products, from specialty chemicals to advanced materials.

InChI:InChI=1/C9H9NO4/c1-6(11)8-4-3-7(14-2)5-9(8)10(12)13/h3-5H,1-2H3

Upstream product

• 50424-96-9 4-methoxy-2-nitro-benzoyl chloride 
• 33844-21-2 2-nitro-4-methoxybenzoic acid 
• 1439930-70-7 (E)-1-(4-methoxy-2-nitrophenyl)ethanone O-methyl oxime 
• 80965-21-5 (E)-1-(4-methoxyphenyl)ethan-1-one O-methyl oxime 

Downstream Products

• 42465-53-2 1-(2-amino-4-methoxyphenyl)ethanone 
• 74599-33-0 (E)-1-(4-Methoxy-2-nitro-phenyl)-3-p-tolyl-propenone 
• 74599-31-8 (E)-3-(4-Chloro-phenyl)-1-(4-methoxy-2-nitro-phenyl)-propenone 
• 74599-30-7 (E)-1-(4-Methoxy-2-nitro-phenyl)-3-phenyl-propenone 
• 74599-32-9 (E)-1-(4-Methoxy-2-nitro-phenyl)-3-(4-methoxy-phenyl)-propenone 
• 74625-91-5 6-Methoxy-2-phenylisatogen 
• 25421-26-5 6-methoxy-2-(4-methoxyphenyl)-1-oxyindol-3-one 
• 74625-93-7 6-Methoxy-1-oxy-2-p-tolyl-indol-3-one 
• 74625-92-6 2-(4-chlorophenyl)-6-methoxy-1-oxy-indol-3-one 
• 74599-16-9 (4-Methoxy-2-nitro-phenyl)-(3-phenyl-oxiranyl)-methanone 
• 74625-98-2 3-(4-Methoxy-2-nitro-phenyl)-3-oxo-2-phenyl-propionaldehyde 
• 74599-19-2 (4-Methoxy-2-nitro-phenyl)-(3-p-tolyl-oxiranyl)-methanone 
• 74599-06-7 3-(4-Methoxy-2-nitro-phenyl)-3-oxo-2-p-tolyl-propionaldehyde 
• 74599-17-0 [3-(4-Chloro-phenyl)-oxiranyl]-(4-methoxy-2-nitro-phenyl)-methanone 

Relevant academic research and scientific papers

Palladium-catalyzed chelation-assisted aromatic C-H nitration: Regiospecific synthesis of nitroarenes free from the effect of the orientation rules

A palladium-catalyzed chelation-assisted ortho-nitration of aryl C-H bond is described. A range of azaarenes such as 2-arylquinoxalines, pyridines, quinoline, and pyrazoles were nitrated with excellent chemo- and regioselectivity. Using the O-methyl oximyl group as a removable directing group, the regiospecific synthesis of a variety of o-nitro aryl ketones was achieved starting from aryl ketones via a three-step process involving the Pd-catalyzed ipso-nitration of C-H bond as a key step. Mechanistic investigations support a silver-mediated radical mechanism involving Pd((II/III) and/or Pd(II/IV) catalytic cycles under oxidizing conditions.