116441-78-2

Usage

Uses

Used in Pharmaceutical Industry:
Ethanone, 1-[5-(3,4-dimethoxyphenyl)-2-methyl-3-furanyl]is used as a pharmaceutical intermediate for the synthesis of various drugs. Its unique chemical structure allows it to serve as a key component in the development of new therapeutic agents.
Used in Medicinal Chemistry Research:
Due to its potential therapeutic applications and ability to interact with biological systems, Ethanone, 1-[5-(3,4-dimethoxyphenyl)-2-methyl-3-furanyl]is used in medicinal chemistry research to explore its properties and identify possible medical uses. This includes investigating its interactions with biological targets and evaluating its efficacy in treating specific conditions or diseases.

Upstream product

• 5703-21-9 3,4-dimethoxyphenylacetaldehyde 
• 123-54-6 acetylacetone 
• 131581-41-4 1,1-difluoro-2-(3,4-dimethoxyphenyl)ethene 
• 29397-21-5 Diacetyldiazomethan 
• 4302-52-7 4-ethynylveratrole 

Relevant academic research and scientific papers

Auto-Tandem Catalysis-Induced Synthesis of Trisubstituted Furans through Domino Acid-Acid-Catalyzed Reaction of Aliphatic Aldehydes and 1,3-Dicarbonyl Compounds by using N-Bromosuccinimide as Oxidant

A simple aluminium(III) chloride-catalyzed synthesis of tri-substituted furans from aliphatic aldehydes and 1,3-dicarbonyl compounds was developed by using N-bromosuccinimide (NBS) as an oxidant. This method was effective for the synthesis of various furan derivatives. Some of the products were not accessible with the previously reported methods. Mechanically, this reaction involved an auto-tandem catalysis based on a newly reported acid-acid-catalyzed tandem reaction to ensure that furans were successfully synthesized. (Figure presented.).

By accompanies two fluorine olefin preparing multi-substituted furan derivatives

The invention relates to a method for preparation of a polysubstituted furan derivative, the method comprises the following main steps: in the presence of a copper salt and an oxyacid salt of an IA element in the element periodic table, gem-difluoroolefin

Copper-catalyzed coupling cyclization of gem -difluoroalkenes with activated methylene carbonyl compounds: Facile domino access to polysubstituted furans

A novel and efficient CuI-catalyzed synthesis of 2,3,5-trisubstituted furans was developed via coupling cyclization of gem-difluoroalkenes with active methylene carbonyl compounds such as 1,3-dicarbonyl compounds, acetoacetonitrile, and phenylsulfonylacet

DIRECT SYNTHESIS OF FURANS BY 3 + 2 CYCLOADDITIONS BETWEEN RHODIUM(II) ACETATE STABILIZED CARBENOIDS AND ACETYLENES

When appropriate substituents are used, rhodium(II) acetate catalyzed decomposition of diazocarbonyls in the presence of acetylenes results in the formation of furans, derived from dipolar intermediates.