35031-72-2

Usage

Uses

Used in Pharmaceutical Industry:
4-Ethoxypropiophenone is used as an intermediate in the synthesis of various pharmaceuticals for its ability to facilitate the production of complex organic compounds.
Used in Food Industry:
4-Ethoxypropiophenone is used as a reagent in the production of certain food additives and flavorings due to its compatibility with organic compounds and its role in synthesis processes.
It is important to handle 4-ethoxypropiophenone with caution, as it can be irritating to the skin, eyes, and respiratory system.

InChI:InChI=1/C11H14O2/c1-3-11(12)9-5-7-10(8-6-9)13-4-2/h5-8H,3-4H2,1-2H3

Upstream product

• 79-03-8 propionyl chloride 
• 103-73-1 Phenetole 
• 123-62-6 propionic acid anhydride 
• 108-24-7 acetic anhydride 

Downstream Products

• 619-86-3 4-(ethoxy)benzoic acid 
• 1031927-88-4 1-(4-ethoxy-phenyl)-propan-1-ol 
• 91247-25-5 1-(4-ethoxy-phenyl)-propan-1-one oxime 
• 26129-26-0 C₁₁H₁₃NO₃ 
• 854651-48-2 1-(4-ethoxyphenyl)propane-1,2-dione 
• 1202873-82-2 C₂₄H₂₇N₃O₅ 
• 1202873-92-4 C₂₄H₂₈N₄O₄ 
• 1202873-69-5 C₁₃H₁₆N₂O₂ 
• 1225999-08-5 C₁₃H₁₆O₄ 

Relevant academic research and scientific papers

BR?NSTED-ACIDIC FLUOROALKYL PHOSPHONATES

The invention relates to Br?nsted-acidic fluoroalkyl phosphonates as bifunctional catalysts and to processes for the preparation thereof.

Etherification of darylmethanols and 1-phenylalkan-1-ols over platinum on carbon

In the presence of platinum on carbon (Pt/C), diarylmethanols and donor substituted 1-phenylalkan-1-ols undergo cross-etherification with primary and secondary alcohols.

Catalytic Friedel-Crafts acylation of alkoxy benzenes by ferric hydrogensulfate

Friedel-Crafts acylation of alkoxy benzenes is achieved efficiently by reaction with aliphatic acid anhydrides in the presence of catalytic amounts of ferric hydrogensulfate, Fe(HSO4)3, in nitromethane. Alkyl benzenes and aryl halides, as well as aromatic anhydrides, remain intact under these conditions.

Catalytic Friedel-Crafts acylation of alkoxybenzenes mediated by aluminum hydrogensulfate in solution and solvent-free conditions

Friedel-Crafts acylation of alkoxybenzenes was achieved efficiently by a reaction with aliphatic acid anhydrides in the presence of catalytic amounts of aluminum hydrogensulfate, Al(HSO4)3, in nitromethane and under solvent-free conditions. Alkylbenzenes and aryl halides, as well as aromatic anhydrides, remained intact under these conditions.