2123-56-0

Usage

Uses

Used in Chemical Synthesis:
Ethanone, 1-(2-methoxy-5-methylphenyl)-2-phenyl-, is utilized as a key intermediate in the synthesis of various organic compounds. Its unique structure allows it to participate in a variety of chemical reactions, making it a valuable component in the creation of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, Ethanone, 1-(2-methoxy-5-methylphenyl)-2-phenyl-, serves as a building block for the development of new drugs. Its specific structural features may contribute to the design of molecules with novel therapeutic properties, potentially leading to the discovery of treatments for various diseases and conditions.
Used in Flavor and Fragrance Industry:
Due to its aromatic nature, Ethanone, 1-(2-methoxy-5-methylphenyl)-2-phenyl-, may be employed in the flavor and fragrance industry. Its unique scent profile could be used to create distinctive fragrances for perfumes, cosmetics, and other consumer products.
Used in Material Science:
Ethanone, 1-(2-methoxy-5-methylphenyl)-2-phenyl-, may also find applications in material science, particularly in the development of new polymers and coatings. Its chemical properties could influence the physical characteristics of these materials, such as their durability, stability, and resistance to environmental factors.

Upstream product

• 103-82-2 phenylacetic acid 
• 104-93-8 p-methylanizole 
• 74-88-4 methyl iodide 
• 103-80-0 phenylacetyl chloride 

Downstream Products

• 114508-52-0 1-(2-methoxy-5-methyl)-2-phenylethylamine 
• 111289-00-0 C₄₃H₃₂O₂ 
• 111288-98-3 8-(1-methoxy-m-tolyl)-7,9,10-triphenylfluoranthene 
• 104450-84-2 3-(p-Methoxytolyl)-2,4,5-triphenylcyclopentadienone 
• 104450-86-4 2-Methoxy-5-methyl-benzil 

Relevant academic research and scientific papers

Aluminum dodecatungstophosphate (AlPW12O40) as a non-hygroscopic Lewis acid catalyst for the efficient Friedel-Crafts acylation of aromatic compounds under solvent-less conditions

Stable and non-hygroscopic aluminum dodecatungstophosphate (AlPW 12O40), which is prepared easily from cheap and commercially available compounds was found to be an effective catalyst for Friedel-Crafts acylation reactions using carboxylic acids, acetic anhydride and benzoyl chloride in the absence of solvent under mild reaction conditions.

Synthesis of Some New Polynuclear Compounds by Cycloaddition Reaction

A large number of 7,9-disubstituted derivatives (I) of cyclopentacenaphthylene-8(H)-one and 2,5-disubstituted derivatives (II) of 3,4-diphenylcyclopentadienone have been synthesized by condensing acenaphthaquinone and benzil separately with suitable 1,3-disubstituted propan-2-ones.The 3-(o- and p-methoxytolyl)cyclopentadienones (IX) have been synthesized by Friedel-Crafts reaction of appropriate methyl cresyl ethers and phenacyl chloride.These dienones have been subjected to Diels-Alder reaction with acenaphthylene and a new acetylenic dienophile (V) (whose synthesis is also described in this paper) to yield a large number of polynuclear aromatic compounds having fluoranthene and p-quaterphenyl nuclei, which have been finally characterised by elemental analyses, IR and PMR spectral data.

Synthesis of Some Polyphenylated Aromatic Compounds Using Tetracyclone Derivatives

The 3-(o- and p-methoxytolyl)-2,4,5-triphenylcyclopentadienones (I) have been synthesised and subjected to Diels-Alder reaction with diphenylacetylene and bicyclo-hepta-2,5-diene to give the polyphenylated aromatic hydrocarbons.The products have been characterised by elemental analyses, IR, PMR and UV spectra.