6437-63-4

Usage

Uses

Used in Pharmaceutical Synthesis:
1-(3-METHOXYPHENOXY)-2-PROPANONE is used as an intermediate for the synthesis of pharmaceuticals, contributing to the development of new drugs and medications. Its chemical structure allows it to participate in a range of reactions, making it a valuable component in the creation of diverse pharmaceutical compounds.
Used in Agrochemical Production:
In the agrochemical industry, 1-(3-METHOXYPHENOXY)-2-PROPANONE is utilized as an intermediate in the production of various agrochemicals. Its role in this sector is crucial for the development of compounds that can enhance crop protection and improve agricultural yields.
Used in Organic Compound Preparation:
1-(3-METHOXYPHENOXY)-2-PROPANONE serves as a reagent in the preparation of different organic compounds. Its ability to engage in multiple chemical reactions makes it an essential tool for researchers and chemists working on the synthesis of new organic molecules.
Used in Research and Development:
1-(3-METHOXYPHENOXY)-2-PROPANONE is also used as a building block in research for the development of new compounds with potential biological activities. Its unique structure and reactivity make it a promising candidate for exploring novel applications in various scientific fields.

Upstream product

• 150-19-6 O-methylresorcine 
• 78-95-5 chloroacetone 
• 598-31-2 1-bromoacetone 

Downstream Products

• 29040-52-6 6-methoxy-3-methylbenzofuran 
• 18621-33-5 (3-Methoxy-phenoxy)-aceton-dimethylketal 
• 85276-75-1 N-benzyl-N-[2-(3-methoxyphenoxy)-1-methylethyl]amine 
• 52814-92-3 1-(6-methoxybenzofuran-2-yl)ethan-1-one 
• 10410-28-3 6-methoxy-3-methylbenzofuran-2-carbaldehyde 
• 10410-29-4 6-methoxy-3-methyl-benzofuran-2-carboxylic acid 
• 1655-71-6 (2-methoxy-phenyl)-(3-methoxy-phenyl)-ether 
• 14064-91-6 2,3'-Dimethoxy-5-nitro-diphenylether 
• 14064-96-1 2,3'-Dimethoxy-5-amino-diphenylaether 
• 70959-08-9 5-{1-Hydroxy-2-[2-(3-methoxy-phenoxy)-1-methyl-ethylamino]-ethyl}-2-methyl-benzenesulfonamide; hydrochloride 
• 344755-10-8 5-(2-{Benzyl-[2-(3-methoxy-phenoxy)-1-methyl-ethyl]-amino}-acetyl)-2-methyl-benzenesulfonamide 
• 344755-07-3 5-(2-{Benzyl-[2-(3-methoxy-phenoxy)-1-methyl-ethyl]-amino}-1-hydroxy-ethyl)-2-methyl-benzenesulfonamide 
• 449195-16-8 2-[benzyl[2-(3-methoxyphenoxy)-1-methylethyl]amino]-1-ethanol 
• 868856-47-7 (Z)-4-dimethylamino-3-(3-methoxyphenoxy)-3-buten-2-one 

Relevant academic research and scientific papers

Iridium-catalyzed enantioselective intramolecular hydroarylation of allylic aryl ethers devoid of a directing group on the aryl group

Although intramolecular hydroarylation is an attractive transformation of allylic aryl ethers, it has suffered from narrow substrate scope. We herein describe Ir/(S)-DTBM-SEGPHOS-catalyzed intramolecular hydroarylation of allylic aryl ethers. The reaction

Efficient synthetic approach to substituted benzo[b]furans and benzo[b]thiophenes by iodine-promoted cyclization of enaminones

An efficient synthetic approach to the substituted benzo[b]furan and benzo[b]thiophene scaffolds by iodine-mediated cyclization of the corresponding enaminones is described. This protocol was applied to a large series of these latter precursors to afford the respective benzoheterocycles substituted at the C-2 position by a carbonyl group functionality. A study of the factors that control this process reveals that the reactivity depends on the presence of electron-donor groups in the aryl ring of the aryloxycarbonylic and arylthiocarbonylic moieties.

BCl3-promoted synthesis of benzofurans

Lewis acidic nature of boron trichloride (BCl3) to coordinate to the carbonyl functionality was exploited for the synthesis of benzofurans via dehydrative cyclization. This mild and efficient procedure allowed for facile access to a number of h

An efficient synthesis of benzofurans and their application in the preparation of natural products of the genus Calea

The intramolecular cyclization of the β-substituted olefins methyl 2-aryloxy-3-dimethylaminopropenoates 3a-3f catalyzed by Lewis acids leads to a short and novel synthesis of benzofurans 2a-2f. When the olefins 4-dimethylamino-3-aryloxy-3-buten-2-ones 4a-4f were used, the cyclization process was faster and provided the corresponding substituted 2-acetylbenzofurans 1a-1f. Among the latter, naturally occurring compounds calebertin (1a), caleprunin A (1b), and caleprunin B (1c) were prepared in good overall yields. These benzofurans were also obtained by direct treatment under MW irradiation of the precursors 1-aryloxypropan-2-ones 7a-7c with DMFDMA, followed by addition of the catalyst, resulting in a route that was one step shorter.