75230-41-0

Basic information

• Product Name: 4'-(2-ACETOXYETHOXY)ACETOPHENONE
• Synonyms: 4'-(2-ACETOXYETHOXY)ACETOPHENONE;ACETIC ACID 2-(4-ACETYLPHENOXY)ETHYL ESTER;Acetoxyethoxyacetophenone;Acetic acid 2-(p-acetylphenoxy)ethyl ester;p-(2-Acetoxyethoxy)acetophenone;2-(4-acetylphenoxy)ethyl acetate
• CAS NO: 75230-41-0
• Molecular Formula: C₁₂H₁₄O₄
• Molecular Weight: 222.24
• Mol File: 75230-41-0.mol
• Article Data: 2

Chemical Properties

• Melting Point: 64 °C
• Boiling Point: 338.6 °C at 760 mmHg
• Flash Point: 148.9 °C
• Appearance: /
• Density: 1.122 g/cm³
• CAS DataBase Reference: 4'-(2-ACETOXYETHOXY)ACETOPHENONE(CAS DataBase Reference)
• NIST Chemistry Reference: 4'-(2-ACETOXYETHOXY)ACETOPHENONE(75230-41-0)
• EPA Substance Registry System: 4'-(2-ACETOXYETHOXY)ACETOPHENONE(75230-41-0)

Safety Data

• Hazardous Substances Data: 75230-41-0(Hazardous Substances Data)

Usage

General Description

4'-(2-acetoxyethoxy)acetophenone is a chemical compound with the molecular formula C12H14O4. It is a white crystalline solid that is commonly used in the synthesis of other organic compounds. 4'-(2-ACETOXYETHOXY)ACETOPHENONE is a derivative of acetophenone, with an acetoxyethoxy group attached to the para position of the phenyl ring. It is also known as 4-(2-acetoxyethoxy)acetophenone or 4-acetoxymethoxyacetophenone. This chemical is used in the production of pharmaceuticals, fragrances, and as a chemical intermediate in various industries. It is important to handle this compound with caution as it may pose risks to human health and the environment.

Upstream product

• 31769-45-6 1-(4-(2-hydroxyethoxy)phenyl)ethanone 
• 75-36-5 acetyl chloride 
• 6192-44-5 2-phenoxyethyl acetate 
• 64-19-7 acetic acid 

Downstream Products

• 31769-45-6 1-(4-(2-hydroxyethoxy)phenyl)ethanone 

Relevant articles and documents

Chemoselective and ligand-free aerobic oxidation of benzylic alcohols to carbonyl compounds using alumina-supported mesoporous nickel nanoparticle as an efficient recyclable heterogeneous catalyst

An economically efficient and operationally simple ligand-free protocol for the chemoselective oxidation of benzylic alcohols to carbonyl compounds has been developed using alumina-supported nickel nanoparticles as a stable recyclable heterogeneous catalyst along with potassium tert-butoxide in the presence of aerial oxygen as an eco-friendly oxidant. The aliphatic alcohols remained unaffected under the present condition. Excellent chemoselectivity has also been demonstrated through intermolecular and intramolecular competition experiments. This protocol accommodates a diverse range of substituents with the tolerance of various sensitive moieties during the reaction. The catalyst could be recovered by filtration and reused consecutively without any significant loss in the catalytic activity. Moreover, the heterogeneity of the catalyst has also been established by the “hot filtration method (Sheldon's test)”.