3245-23-6

Basic information

• Product Name: ACETIC ACID 4-ETHYLPHENYL ESTER
• Synonyms: ETHYL-4-PHENYL-MONO ACETATE;ACETIC ACID 4-ETHYLPHENYL ESTER;4-ETHYLPHENYL ACETATE;4-ethyl-phenoacetate;Phenol,4-ethyl-,acetate;p-ethylphenyl acetate;aceticacid4-ethylphenylester96+%;ETHANOICACID,4-ETHYLPHENYLESTER
• CAS NO: 3245-23-6
• Molecular Formula: C₁₀H₁₂O₂
• Molecular Weight: 164.2
• EINECS: 221-818-6
• Product Categories: Organics
• Mol File: 3245-23-6.mol
• Article Data: 30

Chemical Properties

• Boiling Point: 226 °C
• Flash Point: 91.1°C
• Appearance: /
• Density: 1.03
• Vapor Pressure: 0.0551mmHg at 25°C
• Refractive Index: 1.4980-1.5000
• CAS DataBase Reference: ACETIC ACID 4-ETHYLPHENYL ESTER(CAS DataBase Reference)
• NIST Chemistry Reference: ACETIC ACID 4-ETHYLPHENYL ESTER(3245-23-6)
• EPA Substance Registry System: ACETIC ACID 4-ETHYLPHENYL ESTER(3245-23-6)

Safety Data

• Hazardous Substances Data: 3245-23-6(Hazardous Substances Data)

Usage

General Description

ACETIC ACID 4-ETHYLPHENYL ESTER, also known as ethyl 4-acetoxyphenylacetate, is a chemical compound with a molecular formula of C10H12O3. It is an ester formed from acetic acid and 4-ethylphenol. This colorless liquid with a fruity odor is commonly used as a flavoring agent in various food products. It has applications in the manufacturing of fragrances, pharmaceuticals, and as a solvent in organic synthesis. It is also known to have mild toxic effects on human health, and caution should be exercised when handling and using the compound.

InChI:InChI=1/C10H12O2/c1-3-9-4-6-10(7-5-9)12-8(2)11/h4-7H,3H2,1-2H3

Upstream product

• 201230-82-2 carbon monoxide 
• 1515-95-3 p-ethylanisole 
• 74-88-4 methyl iodide 
• 773-99-9 2-naphthaleneethanol 
• 75-36-5 acetyl chloride 
• 2628-16-2 p-acetoxystyrene 
• 3240-34-4 [bis(acetoxy)iodo]benzene 
• 100-41-4 ethylbenzene 
• 123-07-9 4-Ethylphenol 
• 17993-90-7 4-EtC₆H₄OTMS 
• 108-24-7 acetic anhydride 
• 937-30-4 4-ethylacetophenone 
• 13031-43-1 4-acetyloxyacetophenone 

Downstream Products

• 24539-92-2 3-ethyl-6-hydroxyacetophenone 
• 13031-43-1 4-acetyloxyacetophenone 
• 319457-95-9 C₁₉H₂₉NO₄ 
• 329041-69-2 1-(5-ethyl-2-hydroxyphenyl)-3-phenylpropane-1,3-dione 
• 742078-13-3 2-acetyl-1-benzoyloxy-4-ethylbenzene 
• 288401-00-3 6-ethyl-2-phenyl-chromen-4-one 
• 4010-19-9 1-(2-benzoyloxy-5-methylphenyl)-ethanone 
• 29976-82-7 1-(2-hydroxy-5-methylphenyl)-3-phenylpropane-1,3-dione 
• 29976-75-8 6-methylflavone 
• 288401-02-5 6-ethyl-4'-hydroxyflavone 
• 1609282-49-6 C₁₀H₁₁⁽¹⁸⁾FO₂ 
• 1411983-49-7 3-bromo-N′-((6-ethyl-4-oxo-4H-chromen-3-yl)methylene)benzohydrazide 

Relevant articles and documents

An efficient method to prepare aryl acetates by the carbonylation of aryl methyl ethers or phenols

Synthesis of valuable chemicals from lignin based compounds is critical for the application of biomass. Here, we develop a method of preparing aryl acetates by the carbonylation of aryl methyl ethers or phenols under low CO pressure. Good to excellent yields of aryl acetates were obtained using different substrates, and a possible reaction mechanism was proposed by conducting a series of control experiments. This method may provide a potential way for the utilization of lignin.

Selective hydrodeoxygenation of hydroxyacetophenones to ethyl-substituted phenol derivatives using a FeRu?SILP catalyst

The selective hydrodeoxygenation of hydroxyacetophenone derivatives is achieved opening a versatile pathway for the production of valuable substituted ethylphenols from readily available substrates. Bimetallic iron ruthenium nanoparticles immobilized on an imidazolium-based supported ionic liquid phase (Fe25Ru75?SILP) show high activity and stability for a broad range of substrates without acidic co-catalysts. This journal is

New photocatalytic fixed-point deuteration method for carbon-carbon unsaturated bonds

The invention relates to a new photocatalytic fixed-point deuteration method for carbon-carbon unsaturated bonds. The method is characterized in that an olefin or alkyne compound and a deuterium source undergoes a deuteration reaction under the catalysis of a light source and a photocatalyst to obtain a deuterated product, wherein the deuterium source is deuterated water, deuterated alcohol or deuterated acid, and the reaction temperature is between room temperature and 80 DEG C. The fixed-point deuteration reaction of the olefin or alkyne compound is realized under the photocatalysis action of the photocatalyst with environmentally-friendly and cheap deuterated water or a deuteration reagent as a deuterium source to substitute deuterium gas. Compared with traditional deuteration reactions, the method has a higher selectivity, milder reaction conditions and higher economical suitability, and is suitable for large-scale deuterated chemical substance production.